EP3105226A1 - Cyclopropylamine als lsd1-hemmer - Google Patents

Cyclopropylamine als lsd1-hemmer

Info

Publication number
EP3105226A1
EP3105226A1 EP15707007.9A EP15707007A EP3105226A1 EP 3105226 A1 EP3105226 A1 EP 3105226A1 EP 15707007 A EP15707007 A EP 15707007A EP 3105226 A1 EP3105226 A1 EP 3105226A1
Authority
EP
European Patent Office
Prior art keywords
alkyl
piperidin
azetidin
amino
phenylcyclopropyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP15707007.9A
Other languages
English (en)
French (fr)
Other versions
EP3105226B1 (de
Inventor
Fenglei Zhang
Joel R. Courter
Liangxing Wu
Chunhong He
Leah C. Konkol
Ding-Quan Qian
Bo Shen
Wenqing Yao
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Incyte Corp
Original Assignee
Incyte Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=52595463&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP3105226(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to MEP-2019-315A priority Critical patent/ME03580B/de
Priority to EP19190056.2A priority patent/EP3626714A1/de
Priority to RS20191440A priority patent/RS59534B1/sr
Priority to SI201530894T priority patent/SI3105226T1/sl
Priority to PL15707007T priority patent/PL3105226T3/pl
Application filed by Incyte Corp filed Critical Incyte Corp
Publication of EP3105226A1 publication Critical patent/EP3105226A1/de
Publication of EP3105226B1 publication Critical patent/EP3105226B1/de
Application granted granted Critical
Priority to HRP20192033TT priority patent/HRP20192033T1/hr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06—Antianaemics
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/34—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/98—Nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

  • the present invention relates to enzyme inhibitors, which selectively modulate demethylase, and uses therefor.
  • Particular embodiments contemplate compounds and disease indications amenable to treatement by modulation of lysine specific demethylase- 1 (LSDI ). BACKGROUND OF THE INVENTION
  • epigenetic regulators function as cancer drivers or are permissive for tumorigenesis or disease progression. Therefore, deregulated epigenetic regulators are attractive therapeutic targets.
  • LSD 1 lysine specific demethylase- 1
  • HSD 1 histone demethylase
  • N-terminai SWIRM which functions in nucleosome targeting
  • the tower domain which is involved in protein-protein interaction, such as transcriptional co-repressor, co-repressor of REl -silencing transcription factor (CoREST)
  • CoREST REl -silencing transcription factor
  • C terminal catalytic domain whose sequence and structure share homology with the flavin adenine dinucleotide (FAD)-dependent monoamine oxidases (i.e., MAO-A and MAO-B)
  • FAD flavin adenine dinucleotide
  • MAO-A and MAO-B flavin adenine dinucleotide
  • LSDl also shares a fair degree of homology with another lysine specific demethylase (LSD2) (Karytinos, A., et al., A novel mammalian flavin-dependent histone demethylase. J Biol Chem, 2009. 284(26): p. 17775- 82). Although the biochemical mechanism of action is conserved in two isoforms, the substrate specificities are thought to be distinct with relatively small overlap.
  • LSD2 lysine specific demethylase
  • LSD 1/2 mono- and di -methylated at the position of 4 or 9 of histone 3 (H3K4 or H3K9).
  • H3K4 or H3K9 histone 3
  • These mechanisms make LSD 1/2 distinct from other histone demethylase families (i.e. Jumonji domain containing family) that can demethylate mono-, di-, and Iri-methylated lysines through alpha-ketoglutarate dependent reactions (Kooistra, S,M. and K. Helin, Molecular mechanisms and potential functions ofhistone demethyiases. Nat Rev Mol Cell Biol, 2 12. 13(5): p. 297-311; Mosamrnaparast, N. and Y. Shi, Reversal ofhistone methylation:
  • Methylated histone marks on K3K4 and H3K9 are generally coupled with transcriptional activation and repression, respectively.
  • corepressor complexes e.g., CoREST
  • LSDl has been reported to demethylate H3K4 and repress transcription
  • LSD l in nuclear hormone receptor complex (e.g., androgen receptor)
  • Metzger, E., et al. LSDl demethylates repressive histone marks to promote androgen-receptor-dependent transcription. N ature, 2005. 437(7057): p.
  • LSDl may demethylate non-histone proteins. These include p53 (Huang, J., et al., p53 is regulated by the lysine demethylase LSDl . Nature, 2007. 449(7158): p.
  • E2F Kontaki, H. and 1. Talianidis, Lysine methylation regulates E2F1 -induced cell death. Mol Cell, 2010. 39(1): p. 152-60
  • STAT3 Yamamoto, J., et al., Reversible methylation of promoter-bound STATS by histone-modifying enzymes. Proc Natl Acad Sci U S A, 2010. 107(50): p. 21499-504
  • Tat Sakane, N., ei al., Activation of HIY transcription by the viral Tat protein requires a demethylation step mediated by fysine-specific demethylase 1 (LSD 1/KDMl) .
  • PLoS Pathog, 201 1 . 7(8): p. el002184), and myosin phosphatase target subunit 1 (MYPTl) (Cho, H.S., et al., Demethylation of RB regulator MYPTl by histone demethylase LSD J promotes cell cycle progression in cancer cells. Cancer Res, 2011. 71(3): p. 655-60).
  • the lists of non-histone substrates are growing with technical advances in functional proteomics studies. These suggest additional oncogenic roles of LSD 1 beyond in regulating chromatin remodeling.
  • LSD 1 also associates with other epigenetic regulators, such as DNA methyltransferase i (DNMT1) (Wang, I, et al..
  • the lysine demethylase LSD1 (KDM1) is required for maintenance of global DNA methylation. Nat Genet, 2009. 41 (1 ): p. 125-9) and histone deacetylases (FiDACs) complexes (Hakimi, MA, et al., A core-BRAF35 complex containing histone deacetylase mediates repression of neuronal-specific genes. Proc Natl Acad Set Li S A, 2002. 99(11): p. 7420-5; Lee, M.G., et al, Functional interplay between histone demethylase and deacetylase enzymes. Mol Cell Biol, 2006. 26(17): p.
  • LSD1 has been reported to contribute to a variety of biological processes, including ceil proliferation, epithelial-mesenchymal transition (EMT), and stem cell biology (both embryonic stem cells and cancer stem cells) or self-renewal and cellular transformation of somatic cells (Chen, Y., et al., Lysine-specific histone demethylase 1 (LSD1): A potential molecular target for tumor therapy. Crit Rev Eukaryot Gene Expr, 2012. 22(1): p. 53-9; Sun, G., et al., Histone demethylase LSD! regulates neural stem cell proliferation. Mol Cell Biol, 2010. 30(8): p. 1997-2005; Adamo, A., M.J. Barrero, and J.C.
  • This feature may render cancer cells more resistant to conventional therapies, such as chemotherapy or radiotherapy, and then develop recurrence after treatment (Clevers, H., The cancer stem, cell: premises, promises and challenges, Nat Med, 201 1 , 17(3): p. 313-9; Beck, B. and C. Blanpain, Unravelling cancer stem cell potential. Nat Rev Cancer, 2013. 13(10): p. 727-38). LSDl was reported to maintain an undifferentiated tumor initiating or cancer stern cell phenotype in a spectrum of cancers
  • AMLs Acute myeloid leukemias
  • LSC leukemia stem cell
  • LSDl may regulate a subset of genes involved in multiple oncogenic programs to maintain LSC
  • Chondeau, W.J., et al. The histone demethylase KDM1A sustains the oncogenic potential of MLL-AF9 leukemia stem cells. Cancer Cell, 2012. 21(4): p. 473-87; Schenk, T., et al., Inhibition of the LSDl (KDM1A) demethylase reactivates the all-trans-reiinoic acid differentiation pathway in acute myeloid leukemia. Nat Med, 2012. 18(4): p. 605-1 1 ).
  • LSDl Overexpression of LSDl is frequently observed in many types of cancers, including bladder cancer, NSCLC, breast carcinomas, ovary cancer, glioma, colorectal cancer, sarcoma including chondrosarcoma, E ing's sarcoma, osteosarcoma, and rhabdomyosarcoma, neuroblastoma, prostate cancer, esophageal squamous cell carcinoma, and papillary thyroid carcinoma.
  • studies found over-expression of LSDl was significantly associated with clinically aggressive cancers, for example, recurrent prostate cancer, NSCLC, glioma, breast, colon cancer, ovary cancer, esophageal squamous cell carcinoma, and neuroblastoma.
  • LSDl Lysine-specifc demethylase 1
  • CD86 expression is a marker of maturation of dendritic cells (DCs) which are involved in antitumor immune response.
  • DCs dendritic cells
  • CD86 functions as a co-stimulatory factor to activate T cell proliferation (Greaves, P. and J.G. Gribben, The role of B7 family molecules in hematologic malignancy. Blood, 2013. 121(5): p. 734-44; Chen, L. and D.B. Flies, Molecular mechanisms of T cell co-stimulation and co- inhibition. Nat Rev Immunol, 2013. 13(4): p. 227-42).
  • LSDl activity has also been associated with viral pathogenesis.
  • LSD l activity appears to be linked with viral replications and expressions of viral genes.
  • LSDl functions as a co-activator to induce gene expression from the viral immediate early genes of various type of herpes virus including herpes simplex virus (HSV), varicella zoster vims (VZV), and ⁇ -herpesvirus human cytomegalovirus (Liang, Y., et al., Targeting the JMJD2 histone demethylases to
  • ⁇ -globinopathies including ⁇ -thalassemia and sickle cell disease where the production of normal ⁇ -globin, a component of adult hemoglobin, is impaired (Sankaran, V.G. and S.H. Orkin, The switch from fetal to adult hemoglobin. Cold Spring Harb Perspect Med, 2013.
  • LSDl inhibition may potentiate other clinically used therapies, such as hydroxyurea or azacitidine. These agents may act, at least in part, by increasing ⁇ -globin gene expression through different mechanisms.
  • LSDl contributes to tumor development by altering epigenetic marks on histones and non-histone proteins. Accumulating data have validated that either genetic depletio or pharmacological intervention of LSDl normalizes altered gene expressions, thereby inducing differenti tion programs into mature cell types, decreasing cell proliferation, and promoting apoptosis in cancer cells. Therefore, LSDl inhibitors alone or in combination with established therapeutic drugs would be effective to treat the diseases associated with LSDl activity.
  • the present invention is directed to, inter alia, a compound of Formula I:
  • the present invention is farther directed to a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of Formula I and at least one pharmaceutically acceptable carrier.
  • the present invention is further directed to a method of inhibiting LSD 1 comprising contacting the LSD1 with a compound of Formula I.
  • the present invention is further directed to a method of treating an LSD 1 -mediated disease in a patient comprising administering to the patient a therapeutically effective amount of a compound of Formula I.
  • the present invention provides, inter alia, LSD 1 -inhibiting compounds such as a compound of Formula I:
  • ring A is Ce-io ryl or 5-10 membered heteroaryf comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S;
  • ring B is 4-10 membered heterocycloalkyl comprising carbon and 1, 2, or 3 heteroatoms selected from N, O, and S;
  • ring C is ( 1) monocyclic C3-7 cycloalkyl, (2) monocyclic 4-7 membered
  • heterocycloalkyl comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S, or (3) a fused bicyciic moiety havin
  • ring C I is C5-6 cycloalkyl or 5-6 membered heterocycloalkyl comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S;
  • ring C2 is (1 ) phenyl, (2) C5-6 cycloalkyl, (3) 5-6 membered heteroaryl comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S, or (4) 5-6 membered heterocycloalkyl comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from IN, O, and S;
  • each R ! is independently selected from halo, Cj -6 alkyl, C2-6 alkenyi, C2-6 alkynyl, Ci-6 haloalkyl, Ce-io aryl, C3- 10 cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered
  • heterocycloalkyl C6-10 aryl-Ci-4 alkyl-, C3-io cycloalky1-Ci- alkyl-, (5- 1 membered heteroaryl)-Ci-4 alkyl-, (4- 10 membered heterocycloalkyl)-Ci-4 alkyl-, CN, NO2, OR .
  • Ci-e alkyl is optionally substituted with 1 , 2, or 3 substituents independently selected from halo, CN, OR al , SR a! , C(0)R f , C(0)NR cf R d! , C(0)OR a! , OC(0)R M ,
  • each R 2 is substituted on any ring-forming atom of ring B except the ring- forming atom of ring B to which R z is bonded;
  • each R 3 is independently selected from halo, Ci-6 alkyl, C2-5 alkenyl, C2-5 alkynyl, Ci-6 haioaikyl, Gs-io aryl, C3 -10 cycioalkyl, 5- 10 membered heteroaryi, 4- 10 membered
  • R 4 is halo.
  • R 5 and R 6 are each independently selected from H, halo, CN, Cs -4 alkyl, CM
  • R z is H, halo, Ci-6 alkyl, C2-6 alkenyi, C2-6 alkynyl, Ci-6 haloalkyl, Ce- ⁇ aryl, Gs-so cycloalkyl, 5- 10 membered heieroaryl, 4- 10 membered heterocycloalkyl, C0 0 aryl-Ci-4 alkyl- , Cj-io cycloalkyl-Ci-4 alky]-, (5- 10 membered heteroaryl)-Ci-4 alkyl-, (4-10 membered heterocycloalkyl)-Ci-4 alkyl-, CN, NO2, OR 84 , SR a4 , C(0)R M , C(0) R c4 R d4 , C(0)OR a4 , ⁇ ⁇ (.
  • each R a , R b , R c , R d , R a2 , R 2 , R c2 , R d2 , R 83 , R 3 , R c3 , R d3 , R a4 , R 4 , R 04 , and R d4 is independently selected from H, Ci-6 alkyl, Ci -4 haloalkyl, C2-6 alkenyi, C2-6 alkynyl, Ce-io ary , C3-10 cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered heterocycloalkyl, Ce- ⁇ aryl-C i-4 alkyl-, C3-10 cycloalkyl-Ci-4 alkyl-, (5- 10 membered heteroaryl)-CM alkyl-, and (4- 10 membered heterocycloalkyl)-Cf alkyl-, wherein said Ci-6 alkyl, C2-6 alkenyi, C2-6
  • R c and R d together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1 , 2, or 3 substituents independently selected from Ci-6 alkyl, C3-7 cycloalkyl, 4-7 membered heterocycloalkyl, C «-io aryl, 5-6 membered heteroaryl, Ci -5 haloalkyl, halo, CN, OR 35 , SR a5 , C(0)R b5 , C(0)NR e R d5 , C(0)QR a5 , OC(0)R b5 , OC(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R 5 , NR c5 C(0)NR c5 R d5 ,
  • NR c5 QO)OR a3 (. ' ( ⁇ - -)M - R' : -. NR c5 C(-NR e5 )NR c5 R d5 , 8(0)R 5 , S(0)NR c5 R d5 , S(0)?.R b5 , NR c5 S(0) 2 R b5 , NR 5 S(0) 2 NR c5 R d5 , and S(0) 2 R c5 R d5 , wherein said Ci-6 alkyl, C3-7 cycloalkyl, 4-7 membered heterocycloalkyl, Ce-io aryl, and 5-6 membered heteroaryl are optionally substituted by 1, 2, or 3 substituents independently selected from halo, Ci- alkyl, Ci- haloalkyl, Ci- cyanoalkyl, CN, OIK. SR a5 , C(0)R 5 , C(0)NR c5 R 5 ,
  • R c2 and R c2 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from Ci-6 alkyl, C3-7 cycloalkyl, 4-7 membered heterocycloalkyl, Ce-io aryl, and 5-6 membered heteroaryl, Ci-6 haloalkyl, halo, CN, OR a5 , SR a5 , C(0)R b5 ,
  • Ci-6 alkyl, C3-7 cycloalkyl, 4-7 membered heterocycloalkyl, Ce-io aryl, and 5-6 membered heteroaryl are optionally substituted by I, 2, or 3 substituents independently selected from halo, Ci -4 alkyl, CM haloalkyl, CM cyanoalkyl, CN, OR" 5 , SR a ⁇ C(0)R b5 , C(0)NR c5 R
  • R cJ and R d ' together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1 , 2, or 3 substituents independently selected from Ci-6 alkyl, C3-7 cycloalkyl, 4-7 membered heterocycloalkyl, Ce-io aryl 5-6 membered heteroaryl, C 1-6 haloalkyl, halo, CN, OR" 5 , SR a ⁇ C(0)R b5 , C(0)NR c5 R d ⁇ C(0)OR a5 , OC(0)R b5 , OC(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R 5 , NR c5 C(0)NR c5 R d ⁇
  • R 4 and R d4 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered lieterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from Ci-6 alkyl, C3-7 cycloalkyl, 4-7 membered heterocycloalkyl, Ce-io aryl, 5-6 membered heteroaryl, Ci-6 haloalkyl, halo, CN, OR" 5 , SR a ⁇ C(0)R b5 , C(0)NR c5 R d5 , C(0)OR a5 , OC(0)R b5 , OC(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R 5 , NR c5 C(0)NR c5 R d5 ,
  • each R a5 , R b5 , R C5 , and R DS is independently selected from H, CM alkyl, C M haloalkyl, C2- alkenyl, and C2-4 alkynyl, wherein said Ci-4 alkyl, C2-4 aikenyl, and C2-4 alkynyl, is optionally substituted with 1, 2, or 3 substituents independently selected from OH, CN, amino, halo, CM alky], C alkoxy, C1-4 alkylthio, Ci4 alkylamino, di(Ci-4 alkyl)amino, CM haloalkyl, and CM haloalkoxy; and
  • each R E , R EI , R E2 , R e3 , R e4 , and R E5 is independently selected from H, CM alkyl, and
  • n 0, I, or 2;
  • q 0, i, or 2.
  • ring B is monocyclic 4-7 membered heterocycloalkyl comprising carbon and i, 2, or 3 heteroatoms selected from N, O, and S.
  • ring B is a 4- 10 membered heterocycloalkyl comprising carbon and 1, 2, or 3 heteroatoms selected from N, O, and S wherein said ring B comprises at least one ring-forming N atom.
  • ring B is a 4-7 membered heterocycloalkyl comprising carbon and 1, 2, or 3 heteroatoms selected from N, O, and S wherein said ring B comprises at least one ring-forming N atom.
  • ring B is a 6-membered heterocycloalkyl ring comprising carbon and 1 or 2 heteroatoms selected from N, O, and S wherein said ring B comprises at least one ring-forming N atom.
  • ring B is azeiidine or piperidine.
  • ring B is azeiidine.
  • ring B is piperidine.
  • ring C is bound to a ring-forming N atom of ring B.
  • ring A is Gs-io aryl or 5-10 membered heteroaryl having carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S.
  • ring B is 4- 10 membered heterocycloalkyl haying carbon and 1 , 2, or 3 heteroatoms selected from N, O, and S.
  • ring C is (1) monocyclic C3-7 cycloalkyl, (2) monocyclic 4-7 membered heterocycloalkyl having carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S, or (3) a fused bicyclic moiety
  • ring CI is C5-6 cycloalkyl or 5-6 membered heterocycloalkyl haying carbon and 1, 2, 3 or 4 heteroatoms selected from N, O, and S;
  • ring C2 is ( 1) phenyl. (2) Cs-6 cycloalkyl, (3) 5-6 rnernbered heteroaryl having carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and 8, or (4) 5-6 rnernbered heterocycloalkyl having carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S.
  • the compounds of the invention include a compound of Formula II:
  • ring A is Ce-io aryl or 5- 10 rnernbered heteroaryl comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S;
  • ring C is (1) monocyclic C3-7 cycloalkyl, (2) monocyclic 4-7 rnernbered
  • heterocycloalkyl comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S, or (3) a fused bicyclic moiety havin
  • ring C I is Cs-6 cycloalkyl or 5-6 rnernbered heterocycloalkyl comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S;
  • ring C2 is (1) phenyl, (2) Cs-6 cycloalkyl, (3) 5-6 rnernbered heteroaryl comprising carbo and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S, or (4) 5-6 rnernbered heterocycloalkyl comprising carbon and I , 2, 3 or 4 heteroatoms selected from N, O, and 8;
  • X is - i. ' i b - or - C i - i ' i b - :
  • Y is - ⁇ . ⁇ ⁇ .- - or -CH2-CH2-; each R' is independently selected from halo, Ci-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, Ci-6 haloalkyl, Ce-io aryl, Cs-io cycloalkyl, 5- 10 membered heteroaryl, 4 - 10 membered
  • NR c C(0)OR a NR c C(0)NR c R d , NR c S(0)R b , NR c S(0)2R b , NR c S(Oj2NR c R d , S(0)R b , S(0)NR c R d , S(0)jR b , and S(0)2.
  • NR c R d
  • each R 2 is independently selected from halo, Ci- alkyl, CN, OR a! , C(0)R bi ,
  • Ci-6 alkyl is optionally substituted with 1 , 2, or 3 substituents independently selected from halo, CN, OR aS , SR a! , C(0)R i , C(0)NR cf R d! , C(0)OR a! , OC(0)R M ,
  • each R 2 is substituted any ring-forming carbon atom of the ring in Formula II containing X and Y except the ring- forming carbon atom to which R z is bonded;
  • each R 3 is independently selected from halo, Ci-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, Ci-6 haloalkyl, Ce-io ryl, Cs-io cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered
  • heterocycloalkyl Cs-io aryl-Cw alkyl-, C3-10 cycloalkyl-Ci-4 alkyl-, (5-10 membered heteroaryl)-Ci-.4 alkyl-, (4-10 membered heterocycloalkyl)-Ci alkyl-, CN, NO2, OR 82 , SR a2 , C(0)R b2 , C(0)NR c2 R d2 , C(0)OR a2 , OC(0)R b2 , OC(0)NR c2 R d2 , NR c2 R d2 , NR c2 C(0)R 2 , NR c2 C(0)OR a2 , NR c2 C(0)NR c2 R d2 , C(-NR e2 )R b2 , C(-NR e2 )NR c2 R d2 , NR c2 C(-NR s2 )NR c2 R d
  • R 4 is halo, Ci-6 alkyl, C2-0 alkenyl, C2-6 alkynyl, Ci-6 haloalkyl, Gs-io aryl, C3-10 cyeloalkyl, 5- 10 membered heteroaryl, 4- 10 membered heterocycloalkyi, Ce-!o aryl-C alkyl- , C3-10 cycloalkyl-Ci-4 alkyl-, (5- 10 membered heteroaryl)-CM alkyl-, (4-10 membered heterocyeloalkylVCi -4 alkyl-, CN, NO2, OR 83 , SR Ii3 , C(0)R b3 , C(0)NR c3 R d3 , C(0)OR ;i3 , OC(0)R b3 , 0C(0)NR c3 R d3 , NR c3 R d3 , NR c3 C(0)R b3 , NR c3 C(
  • R 5 and R 6 are each independently selected from H, halo, CN, CM alkyl, CM cyanoalkyl, Ci -4 haloalkyl, and -(CM alkyli-OR 35 ;
  • R z is H, halo, Ci-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, Ci-6 haloalkyl, Os-io aryl, Cs-io cyeloalkyl, 5- 10 membered heteroaryl, 4- 10 membered heterocycloalkyi, Ce-io atyl-Ci-4 alkyl- , C3-10 cycloalkyl-Ci-4 alkyl-, (5- 10 membered heteroaryl)-CM alkyl-, (4- 10 membered heterocycloalkyi)-C 1-4 alkyl-, CN, NO?, OR 8 *, SR a4 , C(0)R b4 , C(Q)NR 4 R d4 , C(0)OR a4 , OC(0)R b4 , OC(0)NR c4 R d4 , NR c4 R d4 , NR c4 C(0)R b4 , NR
  • each R 3 , R b , R c , R d , R a2 , R 2 , R c2 , R d2 , R a3 , R b3 , R c3 , R d3 , R a4 , R M , R c4 , and R d4 is independently selected from H, Ci-6 alkyi, Ci -4 haloalkyl, C2-6 alkenyl, C2-6 alkynyl, Ce-jo aryl, Cs- io cycioaikyl, 5- 10 membered heteroaryl, 4- 10 membered heterocycloalkyl, C6-10 aryl-Ci-4 alkyi-, C3-10 cycloalkyl-CM alkyl-, (5- 10 membered heteroaryl)-Ci-4 alkyl-, and (4- 10 membered heterocycloalkyl)-Ct-4 alkyl-, wherein said Ci-6 alkyl, C
  • R c and R d together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1 , 2, or 3 substituents independently selected from Ci-6 alkyl, C3-7 cycioaikyl, 4-7 membered heterocycloalkyl, Ca-io aryl, 5-6 membered heteroaryl, Ci -6 haloalkyl, halo, CN, OR a5 , SR a5 , C(0)R b5 , C(0)NR c5 R d5 , C(0)OR a5 , OC(0)R b5 , 0C(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R 5 , NR c5 C(0)NR c5 R d5 ,
  • cycioaikyl, 4-7 membered heterocycloalkyl, C3 ⁇ 4.io aryl, and 5-6 membered heteroaryl are optionally substituted by 1 , 2, or 3 substituents independently selected from halo, CM alkyl, CM haloalkyl, CM cyanoalkyl, CN, OR" 5 , SR a5 , C(0)R 5 , C(0)NR c5 R d5 , C(0)OR a5 ,
  • R c2 and R oi together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1 , 2, or 3 substituents independently selected from Ci-6 alkyi, Cv?
  • cycioaikyl 4-7 membered heterocycloalkyl, Ce-io aryl, and 5-6 membered heteroaryl, CM haloalkyl, halo, CN, OR 25 , SR 35 , C(Q)R bi , C(0)NR c5 R ds , C(0)OR a5 , OC(0)R 5 , OC(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R b5 ,
  • Ci-6 alkyl, C3-7 cycloalkyl, 4-7 membered heterocydoalkyl, Q-io aryl, and 5-6 membered heteroaryl are optionally substituted by 1, 2, or 3 substituents independently selected from halo, Ci-4 alkyl, Ci -4 haloalkyi, Ci -4 cyanoalkyl,
  • 6-, or 7-membered heterocydoalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from Ci-6 alkyl, C'3-7 cycloalkyl, 4-7 membered heterocydoalkyl, Ce-io aryl, 5-6 membered heteroaryl, C1-0 haloalkyi, halo, CN, OR 35 , SR a5 , C(0)R b5 , C(0)NR e R d5 , C(0)OR aS , OC(0)R b5 , OC(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R 5 , NR c5 C(0)NR c5 R d5 ,
  • R c4 and R c4 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered lieterocycloalkyl group opiionally substituted with 1, 2, or 3 substituents independently selected from Ci-6 alkyl, C'3-7 cycloalkyl, 4-7 membered heterocydoalkyl, Ce-io aryl, 5-6 membered heteroaryl, Ci -6 haloalkyi, halo, CN, OR" 5 , SR a5 , C(0)R 5 , C ' (0)NR c5 R d5 , C(0)QR a5 , ( ) (. ' (( ) jR i . OC(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R b5 , NR c5 C(0)NR c5 R d5 ,
  • each R 115 , R BS , R°, and R d5 is independently selected from H, CM alkyl, CM haloalkyl, C2-4 alkenyl, and C2-4 alkynyl, wherein said Ci-4 alkyl, C2-4 alkenyl, and C2-4 aikynyl, is optionally substituted with 1 , 2, or 3 substituents independently selected from OH, CN, amino, halo, C1-4 alkyl, Ci-4 aikoxy, C1-4 alkylthio, C1-4 alkylamino, di(Ci-4 alkyljamino, C1-4 haloalkyl, and C i-4 haloalkoxy; and
  • each R E , R ei , R E2 , R ei , R &! , and R e5 is independently selected from H, CM alkyl, and
  • n 0, 1 , or 2;
  • n 0, I, 2, or 3;
  • p 0, 1 , 2, 3;
  • the compounds of the invention include a compound of
  • ring A is Ce-io aryl or 5-10 membered heteroaryi comprising carbon and 1, 2, 3 or 4 heteroatoms selected from ⁇ , O, and S;
  • ring C is ( 1) monocyclic C3-7 cycloalkyl, (2) monocyclic 4-7 membered
  • heterocycloalkyl comprising carbon and 1, 2, 3 or 4 heteroatoms selected from , O, and S, or (3) a fased bicyclic moiety havin
  • ring CI is C5-6 cycloalkyl or 5-6 membered heterocycloalkyl comprising carbon and 1, 2, 3 or 4 heteroatoms selected from N, O, and S;
  • ring C2 is (1) phenyl, (2) C5-6 cycloalkyl, (3) 5-6 membered heteroaryi comprising carbon and 1, 2. 3 or 4 heteroatoms selected from N, O, and S, or (4) 5-6 membered heterocycloalkyl comprising carbon and i, 2, 3 or 4 heteroatoms selected from , O, and S;
  • each R' is independently selected from halo, Ci-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, Cue haioaikyl, Ce-io aryl, C3 -10 cycloalkyl, 5-10 membered heteroaryi, 4- 10 membered
  • heterocycloalkyl Gs-io aryl-Ci-4 alkyl-, C3-10 cycloalkyl-Ci-4 alkyl-, (5-10 membered heteroaryi ⁇ -Ci-4 alkyl-, (4-10 membered heterocycloalkyl)-Ci-4 alkyl-, CN, NO2, OR a , SR ⁇ C(0)R , C(0)NR c R d , C(0)OR a , OC(0)R b , OC(0)NR c R d , NR c R d , NR c C(0)R , NR c C(0)OR a ,
  • each R 2 is independently selected from halo, Ci-6 alkyl, CN, OR a! , C(0)R bi ,
  • Ci-6 alkyl is optionally substituted with 1 , 2, or 3 substituents independently selected from halo, CN, OR al , SR a! , C(0)R i , C(0)NR ci R dl , C(0)OR a! , OC(0)R M ,
  • each R 2 is substituted on any ring-forming carbon atom of the azetidine ring depicted in in Formula ilia or the piperidine ring depicted in Formula IHb except the ring- forming carbon atom to which R z is bonded;
  • each R 3 is independently selected from halo, Ci-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, Ci-6 haloalkyl, Ce-io aryl, C3-10 cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered
  • R 4 is halo, Ci-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, Ci-6 haloalkyl, Ce-io ryl, C3- 10 cycloalkyl, 5- 10 membered lieteroaryi, 4- 10 membered heterocycloalkyl, e- ⁇ 0 aiy 1-CM alkyl- , Cj-io cycloalkyl-Ci-4 alkyl-, (5-10 membered heteroaryl)-C!-4 alkyl-, (4-10 membered heterocycloalkyl)-Ci-4 alkyl-, CN, NO2, OR 83 , SR* 3
  • R 5 and R 6 are each independently selected from ⁇ , halo, CN, CM alkyl, CM cyanoalkyl, Ci -4 haloalkyl, and -(C1-4 alkylj-OR" 5 ;
  • R Z is H, halo, Ci-6 alkyl, C2-0 alkenyl, C2-6 alkynyl, Ci-6 haloalkyl, Ce-io ary , Cs-io cycloalkyl, 5- 10 membered heteroarvl, 4- 10 membered heterocycloalkyl, Ce-io aryl-CM alkyl- , Cs-!o cycloalkyl- Ci -4 alkyl-, (5- 10 membered heteroaryl)-Ci-4 alkyl-, (4- 10 membered heterocycloaikyl)-Ci-4 alkyl-, CN, NO2, OR a4 , 8R A4 , C(0)R B4 , C(0)NR E R D4 , C(0)OR a4 , OC(0)R M , OC(0)NR C4 R D4 , NR C4 R D4 , NR c4 C(0)R b4 , NR c4 C(0)OR a4 ,
  • R D2 , R A ⁇ R 3 , R C3 , R D3 , R a4 , R 4 , R C4 , and R D4 is independently selected from H, Ci-6 alkyl, C haloalkyl, C2-6 alkenyl, C2-6 alkynyl, Ce-s o aryl, C3-10 cycloalkyi, 5-10 membered heteroaryi, 4-10 membered heterocycloalkyl, G5-10 aryl-Ci-4 alkyi-, Cvio cycloalkyl-CM alkyl-, (5-10 membered heteroaryl)-Ci-4 alkyl-, and (4-10 membered heterocycloalky1)-Ci-4 alkyl-, wherein said Ci-6 alkyl, C2-6 alkenyl, C2-6 alkyny
  • NR c5 C( NR e5 )NR c5 R d5 , S(0)R 5 , S(0)NR c5 R d5 , 8(0) 2 R 5 , ⁇ R SiOH K ⁇ NR e5 8(0) 2 NR c5 R L ⁇ and S(0) 2 NR c5 R d5 ;
  • R c and R d together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 siibstituents independently selected from Ci-6 alkyl, C3-7 cycloalkyi, 4-7 membered heterocycloalkyl, Ce- so aryl, 5-6 membered heteroaryi, Ci-6 haloalkyl, halo, CN, OR a5 , SR a3 , C(0)R b5 , C(0)NR c5 R d5 , C(0)OR a5 , OC(0)R 5 , OC(0)NR c5 R d5 , NR c5 R d5 , NR ci C(0)R 5 , NR c5 C(0)NR c5 R d5 ,
  • Ci-6 alkyl, C3-7 cycloalkyi, 4-7 membered heterocycioaikyl, Ce- ⁇ aryl, and 5-6 membered heteroaryi are optionally substituted by 1, 2, or 3 siibstituents independently selected from halo, CM alkyi, Ci-4 haloalkyl, CM cyanoalkyl, CN, OR.
  • SR a5 , C(0)R b5 , C(0)NR c5 R d5 , C(0)OR a5
  • 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from Ci-6 alkyl, C3-7 cycloalkyi, 4-7 membered heterocycloalkyl, Ca-io aryl, and 5-6 membered heteroaryi, C ⁇ haloalkyl, halo, CN, OR 35 , SR 35 , C(0)R 5 ,
  • Ci-6 alkyl, C3--7 cycloalkyi, 4-7 membered heterocycloalkyl, C6-10 aryl, and 5-6 membered heteroaryi are optionally substituted by 1, 2, or 3 substituents independently selected from halo, Ci-4 alkyi, CM haloalkyl.
  • R c3 and R J together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocvcloalkyi group opiionally substituted with 1 , 2, or 3 substituents independently selected from Ci-6 alkyl, C3-7 cyeloalkyl, 4-7 membered lieterocycloalkyi, Ce-io aryl, 5-6 membered heteroaryl, Ci -6 haloalkyl, halo, CN, OR A5 , SR a5 , C(0)R b5 , C(O)NR c5 R d5 , C(0)OR a5 , OC(0)R B5 , OC(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R 5 , NR c5 C(0)NR c5 R d5 ,
  • Ci -6 alkyl, C3-7 cyeloalkyl, 4-7 membered lieterocycloalkyi, Ce-io aryl, and 5-6 membered heteroaryl are optionally substituted by 1 , 2, or 3 substituents independently selected from halo, CM alkyl, CM haloalkyl, CM cyanoalkyi, CM, OR 25 , SR a5 , C(0)R 5 , C(0)
  • R c4 and R d4 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered lieterocycloalkyi group optionally substituted with 1 , 2, or 3 substituents independently selected from Ci-6 alkyl, C'3-7 cyeloalkyl, 4-7 membered heterocvcloalkyi, Ce-io aryl, 5-6 membered heteroaryl, Ci -6 haloalkyl, halo, CN, OR 35 , SR a5 , C(0)R b5 , C(0)NR e R d5 , C(0)QR a5 , OC(0)R b5 , OC(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R 5 , NR c5 C(0)NR c5 R d5 ,
  • NR c5 C(0)OR a3 C(-NR e5 )NR c5 R d5 , NR c5 C(-NR e5 )NR c5 R d5 , S(0)R BS , S(0)NR c5 R d5 , S(0) 2 R b5 , NR C5 S(0)2R b5 , R c5 S(0) 2 NR c5 R d5 , and 8(0) 2 NR c5 R d5 , wherein said Ci-6 alkyl, C ' 3-7 cyeloalkyl, 4-7 membered lieterocycloalkyi, Ce-io aryl, and 5-6 membered heteroaryl are optionally substituted by 1 , 2, or 3 substituents independently selected from halo, C alkyl, CM haloalkyl, CM cyanoalkyi, CN, OIK.
  • SR a5 C(0)R 5 , C(0) R C5
  • each R E , R E! , R E2 , R ei , R 84 , and R E5 is independently selected from H, Ci -4 alkyl, and
  • n 0, i, 2, or 3;
  • p 0, 1 , 2, 3;
  • q 0, 1 , or 2.
  • the compounds of the invention include a compound of Formula IV a or IVb:
  • the compounds of the invention include a compound of
  • ring A is Ce-ioaryl or 5-10 membered heteroarvl comprising carbon and 1, 2, 3 or 4 heteroatoms selected from ⁇ , O, and S;
  • ring C is ( 1) monocyclic C3-7 cycloalky], (2) monocyclic 4-7 membered heterocycloalkyl comprising carbon and 1, 2, 3 or 4 heteroatoms selected from , O, and S, or (3) a fused bicyciic moiety havin
  • ring CI is C5-6 cycloalky! or 5-6 membered heterocycloalkyl comprising carbon and 1, 2, 3 or 4 heteroatoms selected from N, O, and S;
  • ring C2 is (1) phenyl, (2) C5-6 cycloalky], (3) 5-6 membered heteroarvl comprising carbon and 1, 2, 3 or 4 heteroatoms selected from , O, and S, or (4) 5-6 membered heterocycloalkyl comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S;
  • each R ! is independently selected from halo.
  • NR c C(0)R , NR c C(0)OR a NR°C(0) R c R d , NR c S(0)R , NR c S(0) 2 R b , NR c S( ' 0)2NR c R d , S(0)R , S(0)NR c R d , S(0) ? .R b , and S(0)2NR c R d ;
  • each R 3 is independently selected from halo, Cs -6 alkyl, C2-6 alkenyl, C2-6 alkynyl, Cs-6 haloalkyl, Ce-io aryl, C3-10 cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered
  • R 4 is halo, Cue alkyl, C2-6 alkenyl, C2-6 alkynyl, Ci- ⁇ s haloalkyl, Ce-io aryl, C3-10 cyeloalkyl, 5- 10 membered Iieteroarvl, 4- i 0 membered heterocycloalkyi, Ce-io aryl-Ci-4 alkyl- , C3-10 cyeloaikyl-Ci-4 alkyl-, (5- 10 membered heieroaryl)-Ci-4 alkyl-, (4- 10 membered heterocycloalkyl)-C alkyl-, CN, O2, OR 33 , SR a3 , C(0)R b3 , C(0)NR c3 R d3 , C(0)OR a3 , OC(Q)R ⁇ OC(0)NR c3 R d3 , NR c3 R d3 , NR c3 C(0)R 3
  • each R a , R , R c , R d , R a2 , R 2 , R c2 , R d2 , R a ⁇ R b3 , R° 3 , and R d3 is independently selected from H, Ci-6 alkyl, C haloalkyl, C2-6 alkenyl, C2-6 alkynyl, Co-io ryl, C3-10 cyeloalkyl, 5- 10 membered heteroaryl, 4- 10 membered heterocycloalkyi, Cs-io aryl-Ci -4 alkyl-, C- O cycloalkyl-Ci-4 alkyl-, (5- 10 membered heteroaryl)-Ci-4 alkyl-, and (4- 10 membered heterocycloalkyl)-Ci -4 alkyl-, wherein said Ci-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, Ce-io aryl, C
  • NR c5 R d5
  • 6-, or 7-membered lieterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from Ci-6 alkyl, C3-7 cyeloalkyl, 4-7 membered lieterocycloalkyl, Gs-io aryl, and 5-6 membered heteroaryl, Ci-6 haloalkyl, halo, CN, OR 23 , SR 35 , C(0)R bi ,
  • Ci-6 alkyl, C3-7 cyeloalkyl, 4-7 membered heterocycloalkyl, Ce-io aryl, and 5-6 membered heteroaryl are optionally substituted by 1, 2, or 3 substituents independently selected from halo, Ci-4 alkyl, CM haloalkyl, CM cyanoalkyl, CN, OR 85 , SR a5 , C(0)R 5 , C(0) R C5 R D5 , ( ' iO )R ⁇ ( ) (.
  • R" and R c3 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from Ci-6 alkyl, C3-7 cyeloalkyl, 4-7 membered heterocycloalkyl, Gs-io aryl, 5-6 membered heteroaryl, Ci -6 haloalkyl, halo, CN, OR AS , SR a5 , C(0)R 5 , C(0)NR c5 R d5 , C(0)GR , ( )(. ' (( ) j i . GC(0)NR c5 R d5 , NR c5 R d5 , NR c5 C(0)R b5 , NR c5 C(0)NR c5 R d5 ,
  • each R a - R 5 , R c5 , and R d " is independently selected from H, Ci-4 alkyl, Ci -4 haloalkyl, C2-4 alkenyl, and C2-4 alkynyl, wherein said Ci-4 alkyl, C2-4 alkenyl, and C2-4 alkynyl, is optionally substituted with 1 , 2, or 3 substituents independently selected from Oil, CN, amino, halo, C 1-4 alkyl, Ci-4 alkoxy, Cs -4 alkylthio, Cs -4 alkylamino, di(Ci 4 alkyl)arnino, C1 -4 haloalkyl, and C 1-4 haloalkoxy; and
  • each R e , R e2 , R 83 , and R e5 is independently selected from II, Ci-4 alkyl, and CN;
  • n 0, i, 2, or 3;
  • p 0, 1 , 2, 3;
  • q 0, 1 , or 2.
  • q is 0.
  • q is 1 .
  • ring A is phenyl
  • n 1
  • R' is halo
  • R' is F.
  • both R 6 and R 6 are H.
  • ring C is monocyclic C3-7 cycloalkyl.
  • ring C is monocyclic 4-7 membered heterocycloalkyl comprising carbon and 1 , 2, 3 or 4 heteroatoms selected from N, O, and S.
  • ring C is cyclopropyl, cyclobutyl, cyclohexyl, azeticlinyl, or piperidinyl.
  • ring C is cyclopropyl, cyclohexyl, azetidiriyl, or piperidinyl.
  • R 4 is Ci-6 alkyl, Ce-io ryi, 5-10 membered heteroaryl, C(0)R 3 , C(O)NR c R d3 , C(0)OR a3 , or S(0) 2 R b3 , wherein said Ci -6 alkyl, Cwo aryl, and 5-10 membered heteroaryl are each optionally substituted with 1 , 2, 3, or 4 substituents independently selected from halo, C1 -4 alkyl.
  • R 4 is Ci-4 alkyl optionally substituted by CN, C(0)NR c3 R d3 , OR 23 , or C(O)OR iL? ,
  • R 4 is Ci -4 alkyl optionally substituted by CN, C(0)NR c3 R d ⁇ or C(0)OR 85 .
  • R 4 is Ci-4 alkyl.
  • R 4 is methyl
  • R 4 is phenyl
  • R 4 is CN
  • R 4 is -CH2-CN.
  • each R 3 is independently selected from Ci-6 alkyl, Ce- 10 aryl, 5- 10 membered heteroaryl, C3-10 cyeioaikyl, 4- 10 membered heteroeycioalkyl, C(0)R b2 , C(0)NR c2 R d2 , C(0)OR a2 , S(0) 2 R 2 , and S(0) 2 NR 2 R d2 , wherein said Ci-6 alley 1, Ce-io ryl, and 5-10 membered heteroaryl, C3-10 cyeioaikyl, 4-10 membered heteroeycioalkyl are each optionally substituted with 1 , 2, 3, or 4 substituents independently selected from halo, C alkyl, CM haloalkyl, CM cyanoalkyL CN, NO?., OR" 2 , SR a2 , C(0)R 2 , C(0)NR c R d2 , C(0)OR e2 ,
  • NR c2 S(0)?.NR c2 R d2 , S(0)R 2 , S(0)NR c2 R d2 , S(0)2R b2 , and S(0)?.NR c2 R d2 .
  • NR c2 S(0)?.NR c2 R d2 , S(0)R 2 , S(0)NR c2 R d2 , S(0)2R b2 , and S(0)?.NR c2 R d2 .
  • each R 3 is independently selected from Ci-6 alkyl, Ce so aryl, 5- 10 membered heteroaryl, C(0)R b2 , C(0)NR c2 R d2 , C(O)0R 3? , and S(0)2R 2 , wherein said Ci-6 alkyl, Ce-io aryl, and 5-10 membered heteroaryl are each optionally substituted with 1 , 2, 3, or 4 substituents independently selected from halo, CM alkyl.
  • each R J is independently selected from Ci-6 alkyl, Ce-io aryl, 5- 10 membered heteroaryi, Cs- io cycloalkyl, 4- 10 membered heterocycloalkyl, C(0)R b2 , C(0)NR c2 R d2 , C(0)OR a2 , S(0)2R B2 , and 8(0)2NR c2 R d2 , wherein said Ci-6 alkyl, Ce-io aryl, 5- 1 0 membered heteroaryi, Cs-io cycloalkyl, and 4- 10 membered heterocycloalkyl are each optionally substituted with 1 , 2, 3, or 4 substituents independently selected from F, CI, CF3, CN, OH, C(0)OH, C(( ) )( ) ( !
  • R z is H, C 1-4 alkyl, or C io aryl-Ci-4 alkyl-, wherein said Ci-4 alkyl and Ce- ⁇ aryl-Cw alkyl- are each optionally substituted by halo or OR a4 .
  • R z is C 1-4 alkyl.
  • R is C1-4 alkyl substituted by methoxy.
  • R is C0-J 0 aryl-Ci-4 alkyl- substituted by fluoro.
  • R z is H, methyl, methoxymethyl, or 4-fluorophenylmethyl.
  • R z is H.
  • p is 0.
  • p is 1.
  • p is 2.
  • m is 0.
  • the compound has a trans configuration with respect to the di- substituted cyclopropyl group depicted in Formula I (or any of Formulas II, Ilia, Illb, IVa, IVb, Va, and Vb).
  • each R a , R , R c , and R d is independently selected from II, Ci-6 alkyl, Ci-4 haloalkyl, C2-6 aikenyl, C2-6 alkynyl, CVio ryl, Cs-so cycloalkyl, 5 - 10 membered heteroaryi, 4- 10 membered heterocycloalkyl, Gs-10 aryl-Ci-4 alkyl-, Cs-so cycloalkyl-Ci-4 alkyl- , (5-10 membered heteroaryl)-Ci-4 alkyl-, and (4- 10 membered heterocyc1oa1kyl)-Ci-4 alkyl-, wherein said C i-6 alkyl, C?. ⁇ 6 aikenyl, C2-6 alkynyl, Ce-to ryl, C3-10 cycloalkyl, 5- 10 membered heteroaryi, 4- 10 membered heterocycloalkyl, Co
  • each R a2 , R 2 , R c2 , and R a2 is independently selected from H, Ci-6 alkyl, Ci-4 haloalkyl, C2-6 alkenyl, C2-6 alkynyl, Ce-io aryl, Gs-10 cycloalkyl, 5- 10 membered heteroaryi, 4- 10 membered heterocycloalkyl, Ce-jo aryl-CM alkyl-, C3-10 cycloalkyl-Ci-4 alkyl-, (5- 10 membered heteroaryl)-Ci-4 alkyl-, and (4- 10 membered heterocycloalkyl)-Ci -4 alkyl-, wherein said C i-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, Ce-io aryl, C3- io cycloalkyl, 5- 10 membered heteroaryi, 4- 10 membered heterocycloalkyl, Ce-io aryl
  • each R a3 , R b3 , R ci , and R d3 is independently selected from H, Ci-6 alkyl, Ci-4 haloalkyl, C2--6 alkenyl, C2-0 alkynyl, Ce-io aryl, C3-10 cycloalkyl, 5- 1 0 membered heteroaryi, 4- 10 membered heterocycloalkyl, G5-10 aryl-C-M alkyl-, C3-10 cycioaikyl-Ci-4 alkyl-, (5- 10 membered heteroaryl)-CM alkyl-, and (4- 10 membered heterocycioaikyl)-Ci--4 alkyl-, wherein said Ci-6 alkyl, C-2 -6 alkenyl, C-2-6 alkynyl, Ce-io aryl, C3- 10 cycloalkyl, 5- 10 membered heteroaryi, 4- 10 membered heterocycio
  • each R &4 , R b4 , R c4 , and R d4 is independently selected from H,
  • each R A , R , R c , and R d is independently selected from II, Ci-6 alkyl, CM haloalkyl, Ce-io aryi, C3 ⁇ 4 -to cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered heterocycloalkyl, Gs-io aryl-CM alkyl-, C3-10 cycloalkyl-Cf-4 alkyl-, (5- 10 membered heteroaryl)-Ci-4 alkyl-, and (4-10 membered heterocycloalkyl)-Ci-4 alkyl-, wherein said Ci-6 alkyl, Gs-io ryl, C3-10 cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered
  • heterocycloalkyl C0- so aryl-Ci-4 alkyl-, C3-10 cycloalkyl-Ci ⁇ alkyl-, (5- 10 membered heteroary])-Ci -4 alkyl-, and (4- 10 membered heterocycloalkyl)-Ci ⁇ 4 alkyl- is optionally substituted with 1 , 2, or 3 substituents independently selected from OH, CN, amino, halo, C M alkyl, Ci-4 alkoxy, Ci 4 alkyithio, Ci .4 alkylamino, di(Ci-4 alkyl)amino, CJ 4 haloalkyl, and C1-4 haioalkoxy.
  • each R a2 , R B2 , R C2 , and R a2 is independently selected from II, Ci-6 alkyl, C1-4 haloalkyl, Ce-io aryl, Cs-so cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered heterocycloalkyl, Gs-10 aryl-Ci -4 alkyl-, C3-10 cycloalkyl-CM alkyl-, (5- 10 membered heteroaryl)-Ci-4 alkyl-, and (4- 1 0 membered heteroeyeioalkyl)-CM alkyl-, wherein said Ci-6 alkyl, Ce-io aryl, C3-10 cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered heterocycloalkyl, Cs-io aryl-CM alkyl-, Cs-so cycloalkyl-Cf-4 alkyl-, (5- 10 membered heteroary
  • each R a3 , R 03 , R c3 , and R d3 is independently selected from H, Cf-6 alkyl, CM haloalkyl, Ce-i 0 aryl, C3-10 cycloalkyl, 5- 10 membered heteroaryl, 4- 10 membered heterocycloalkyl, Co -so aryl-Ci -4 alkyl-, C3-10 cycloalkyl-CM alkyl-, (5- 10 membered heteroaryl)-Ci-4 alkyl-, and (4-10 membered heterocycloalkyl)-Cs -4 alkyl-, wherein said Cs-6 alkyl, Ce- ⁇ aryl, C3-10 cycloalkyl, 5- 10 membered heteroaryl, 4- 1 0 membered heterocycloalkyl, Gs-io aryl-CM alkyl-, C3-10 cycloalkyl-CM alkyl-, (5- 10 membered heteroaryl
  • each R a4 , R M , R c4 , and R c4 is independently selected from II,
  • Ci-4 alkyl Ci-4 alkoxy, C1-4 alkylthio, C1-4 alkylamino, di(Ci-4 alk l)amino, Ci-4 haloalkyl, and CM haioaikoxy.
  • each R a , R b , R c , and R d is independently selected from H and
  • each R a2 , R b2 , R c2 , and R d2 is independently selected from H and Ci-6 alkyl.
  • each R a3 , R 3 , R c3 , and R a3 is independently selected from II and Ci-6 alkyl.
  • each R a4 , R s4 , R c , and R d4 is independently selected from H and Ci-6 alkyl.
  • a floating bond crossing a ring moiety in any structure or formula depicted herein is intended to show, unless otherwise indicated, that the bond can connect to any ring- forming atom of the ring moiety.
  • ring A in Formula I is a naphthyl group
  • an R s substitu ent if present, can be substituted on either of the two rings forming the naphthyl group.
  • ring C is a fused bicyclic moiety of Formula (A)
  • the phrase "wherein said fused bicyclic moiety of Formula (A) is bonded to ring B via ring CI, and wherein Ring C substituents R and R 4 are substituted on either or both of C I and C2" is intended to denote that (1) ring B of Formula I is connected to ring C I and not to ring C2, (2) R 4 is substituted on eit r ring CI or ring C2, and (3) any R 3 that is present is substituted on either ring CI or ring C2.
  • the floating bond over ring CI in Formula (A) is intended to show that ring C I (not ring C2) connects to ring B.
  • the phrase "optionally substituted” means unsubstituted or substituted.
  • substituted means that a hydrogen atom is removed and replaced by a substituent. It is to be understood that substitution at a given atom is limited by valency.
  • Q-j indicates a range which includes the endpoints, wherein i andj are integers and indicate the number of carbons. Examples include Ci-4, Ci -6, and the like.
  • z-membered typically describes the number of ring-forming atoms in a moiety where the number of ring-forming atoms is z.
  • piperidinyl is an example of a 6-membered heteroeycloalkyl ring
  • pyrazoiyl is an example of a 5-membered heteroary i ring
  • pyridyl is an example of a 6-membered heteroaryl ring
  • 4-tetTahydro-naphthalene is an example of a 10-membered cycloalkyl group.
  • carbon refers to one or more carbon atoms.
  • the term "Q-j alkyl,” employed alone or in combination with other terms, refers to a saturated hydrocarbon group that may be straight-chain or branched, having i to j carbons.
  • the alkyl group contains from i to 6 carbon atoms or from 1 to 4 carbon atoms, or from 1 to 3 carbon atoms.
  • alkyl moieties include, but are not limited to, chemical groups such as methyl, ethyl, w-propyl, isopropyl, n-butyl, s- butyl, and t-butyl.
  • Q-j alkoxy employed alone or in combination with other terms, refers to a group of formula -O-alkyl, wherein the alkyl group has i to j carbons.
  • Example alkoxy groups include methoxy, ethoxy, and ropoxy (e.g., n-propoxy and isopropoxy).
  • the alkyl group has i to 3 carbon atoms.
  • Q.j alkenyl employed alone or in combination with other terms, refers to an unsaturated hydrocarbon group having one or more double carbon-carbon bonds and having i to j carbons.
  • the alkenyl moiety contains 2 to 6 or 2 to 4 carbon atoms.
  • Example alkenyl groups include, but are not limited to, ethenyl, w-propenyl, isopropenyl, /2-butcnyl, seobutenyl, and the like.
  • Q-j afkynyl refers to an unsaturated hydrocarbon group having one or more triple carbon-carbon bonds and having i to j carbons.
  • Example alkynyl groups include, but are not limited to, ethynyl, propyn- 1 -yl, propyn-2-yl, and the like. In some embodiments, the alkynyl moiety contains 2 to 6 or 2 to 4 carbon atoms.
  • Ci-j alkylamino,'' employed alone or in combination with other terms refers to a group of formula -NII(alkyl), wherein the alkyl group has i to j carbon atoms. In some embodiments, the alkyl group has I to 6 or 1 to 4 carbon atoms. Exemplary alkylamino groups include methyl amino, ethylamino, and the like.
  • di-G-j-alkylammo refers to a group of formula -N(alkyl) 2 , wherein each of the two alkyl groups has, independently, i to j carbon atoms. In some embodiments, each alkyl group independently has 1 to 6 or 1 to 4 carbon atoms, in some embodiments, the dialkylamino group is -N(Ci- alkyl)?. such as, for example, dimethylamino or diethylamino.
  • Ci-j alkylthio employed alone or in combination with other terms, refers to a group of formula -S-alkyl, wherein the alkyl group has i to j carbon atoms. In some embodiments, the alkyl group has i to 6 or 1 to 4 carbon atoms. In some embodiments, the alkylthio group is Ci -4 alkylthio such as, for example, methylthio or ethylthio.
  • amino employed alone or in combination with other terms, refers to a group of formula -Ni b.
  • aryi refers to a monocyclic or polycyclic (e.g., having 2, 3 or 4 fused rings) aromatic hydrocarbon, such as, but not limited to, phenyl, i-naphthy], 2-naphthyl, anthracenyl, phenantbrenyl, and the like.
  • aryl is Ce-io aryl.
  • the aryl group is a naphthalene ring or phenyl ring.
  • the aryi group is phenyl.
  • carbonyl employed alone or in combination with other terms, refers to a -C(O)- group.
  • Ci-j cyanoalkyl employed alone or in combination with other terms, refers to an alkyl group substituted by a CN group.
  • Cycloaikyl refers to a non-aromatic cyclic hydrocarbon moiety having i to j ring-forming carbon atoms, which may optionally contain one or more alkenvlene groups as part of the ring structure. Cycloaikyl groups can include mono- or polycyclic (e.g., having 2, 3 or 4 fused rings) ring systems.
  • cycloaikyl Also included in the definition of cycloaikyl are moieties that have one or more aromatic rings fused (i.e., having a bond in common with) to the cycloaikyl ring, for example, benzo derivatives of cyclopentane, cyelopentene, cyclohexane, and the like.
  • One or more ring-forming carbon atoms of a cycloalkyl group can be oxidized to form carbonyl linkages.
  • cycloalkyl is C3-10 cycloalkyl, C3-7 cycloalkyl, or C5-0 cycloalkyl.
  • Exemplary cycloalkyl groups include cyclopropyi, cyclobutyi, cyclopentyl, cyclohexyl, cycloheptyl, cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptatrienyl, norborayl, norpinyl, norcamyl, and the like.
  • Further exemplary cycloalkyl groups include cyclopropyi, cyclobutyi, cyclopentyl, and cyclohexyl
  • G-j haioalkoxy refers to a group of formula -G ) -haloalkyl having i to j carbon atoms.
  • An example haioalkoxy group is OCF3.
  • An additional example haioalkoxy group is OCHF2.
  • the haioalkoxy group is iluorinated only.
  • the alkyl group has 1 to 6 or 1 to 4 carbon atoms.
  • the haioalkoxy group is Ci -4 haioalkoxy.
  • halo refers to a halogen atom selected from F, CI, I or Br. In some embodiments, “halo” refers to a halogen atom selected from F, CI, or Br. In some embodiments, the halo substituent is F.
  • G-j haloalkyl refers to an alkyl group having from one halogen atom to 2s+l halogen atoms which may be the same or different, where "s" is the number of carbon atoms in the alkyl group, wherein the alkyl group has i to j carbon atoms.
  • the haloalkyl group is iluorinated only.
  • the haloalkyl group is tluoromethyl, difluoromethyl, or trifluoromethyl.
  • the haloalkyl group is trifluoromethyl.
  • the alkyl group has 1 to 6 or i to 4 carbon atoms.
  • heteroaryl refers to a monocyclic or polycyclic (e.g., having 2, 3 or 4 fused rings) aromatic heterocylic moiety, having one or more heteroatom ring members selected from nitrogen, sulfur and oxygen.
  • the heteroaryl group has 1 , 2, 3, or 4 heteroatom ring members.
  • the heteroaryl group has I , 2, or 3 heteroatom ring members.
  • the heteroaryl group has 1 or 2 heteroatom ring members.
  • the heteroaryl group has 1 heteroatom ring member.
  • the heteroaryl group is 5- to 10-membered or 5- to 6-membered.
  • the heteroaryl group is 5-membered. In some embodiments, the heteroaryl group is 6-membered. When the heteroaryl group contains more than one heteroatom ring member, the heteroatoms may be the same or different. The nitrogen atoms in the ring(s) of the heteroaryl group can be oxidized to form N-oxides.
  • Example heteroaryl groups include, but are not limited to.
  • p ridinyl pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, pyrazolyl, azolyl, oxazolyl, isoxazolvl, thiazolyl, isothiazolyi, imidazoluyl, furanyl, thiophenyl, triazolyl, tetrazolyl, thiadiazolyl, quinolinyl, isoquinolinyl, indoieyl benzothiophenyl, benzofuranyl, benzisoxazolyl, imidazo[l , 2-b]ihiazolyl, purinyl, triazinyl, and the like.
  • a 5-memhered heteroaryl is a heteroaryl group having five ring-forming atoms comprising wherein one or more of the ring-forming atoms are independently selected from N, O, and S.
  • the 5-membered heteroaryl group has 1, 2, or 3 heteroatom ring members.
  • the 5-rnernbered heteroaryl group has 1 or
  • the 5-membered heteroaryl group has 1 heteroatom ring member.
  • Example ring-forming members include CH, N, NH, O, and S.
  • Example five-membered ring heteroaryls are thienyl, furyl, pyrrolyl, imidazolyl, thiazolyl, oxazolyl, pyrazolyl, isothiazolyi, isoxazolvl, I, 2, 3-triazolyl, tetrazolyl, 1 , 2, 3-thiadiazolyl, I, 2, 3-oxadiazolyl, 1, 2, 4-triazolyl, i, 2, 4-thiadiazolyl, i, 2, 4-oxadiazolyl, 1 , 3, 4-triazolyl, 1 , 3, 4-thiadiazoiyl, and 1 , 3, 4-oxadiazolyl.
  • a 6-membered heteroaryl is a heteroaryl group having six ring-forming atoms wherein one or more of the ring-forming atoms is N.
  • the 6-membered heteroaryl group lias 1 , 2, or 3 heteroatom ring members.
  • the 6- membered heteroaryl group has 1 or 2 heteroatom ring members.
  • the 6-membered heteroaryl group has 1 heteroatom ring member.
  • Example ring-forming members include CH and N.
  • Example six-memhered ring heteroaryls are pyridyl, pyrazinyl, pyrimidinyl, triazinyl, and pyridazinyl.
  • heterocycloalkyl employed alone or in combination with other terms, refers to non-aromatic heterocyclic ring system, which may optionally contain one or more unsaturations as part of the ring structure, and which has at least one heteroatom ring member independently selected from nitrogen, sulfur and oxygen.
  • the heterocycloalkyl group has 1 , 2, 3, or 4 heteroatom ring members. In some embodiments, the heterocycloalkyl group has 1, 2, or 3 heteroatom ring members. In some embodiments, the heterocycloalkyl group has 1 or 2 heteroatom ring members. In some embodiments, the heterocycloalkyl group has i heteroatom ring member. When the heterocycloalkyl group contains more than one heteroatom in the ring, the heteroatoms may be the same or different.
  • Example ring-forming members include CH, CFh, C(O), N, NH, O, S, S(0), and 8(0)2, Heterocycloalkyl groups can include mono- or polycyclic (e.g., having 2,
  • heterocycloalkyl 3 or 4 fused rings
  • moieties that have one or more aromatic rings fused (i.e., ha ing a bond in common with) to the non-aromatic ring, for example, 1 , 2. 3, 4-tetrahydro-quinoline, dihydrobenzofuran and the like.
  • the carbon atoms or heteroatoms in the ring(s) of the heterocycloalkyl group can be oxidized to form a carbonyl, sulfinyl, or sulfonyl group (or other oxidized linkage) or a nitrogen atom can be quaternized.
  • the heterocycloalkyl is 5- to 10-membered, 4- to 10-membered, 4- to 7-membered, 5-membered, or 6-membered.
  • heterocycloalkyl groups include i , 2, 3, 4-tetrahydro- quinolinyl, dihydrobenzofuranyl, azetidinyi, azepanyl, pyrroiidinyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, and pyranyl.
  • the compounds described herein can be asymmetric (e.g., having one or more stereocenters). All stereoisomers, such as enantsomers and diastereoisomers, are intended unless otherwise indicated.
  • Compounds of the present invention that contain asymmetrically substituted carbon atoms can be isolated in optically active or racemic forms. Methods on how to prepare optically active forms from optically inactive starting materials are known in the art, such as by resolution of racemic mixtures or by stereoselective synthesis. Many geometric isomers of olefins, C ⁇ N double bonds, and the like can also be present in the compounds described herein, and all such stable isomers are contemplated in the present invention. Cis and trans geometric isomers of the compounds of the present invention are described and may be isolated as a mixture of isomers or as separated isomeric forms.
  • the compounds of the invention when the compounds of the invention contain a chiral center, the compounds can be an of the possible stereoisomers. In compounds with a single chiral center, the
  • stereochemistry of the chiral center can be (R) or (S).
  • the stereochemistry of the chiral centers can each be independently (R) or (S) so the configuration of the chiral centers can be (R) and (R), (R) and (8); (8) and (R), or (S) and (S).
  • each of the three chiral centers can each be independently (R) or (S) so the configuration of the chiral centers can be (R), (R) and (R); (R), (R) and (S); (R), (S) and (R); (R), (S) and (S); (S), (R) and (R); (8), (R) and (S); (S), (S) and (R); or (8), (8) and (8).
  • An example method includes fractional recrystallization using a chiral resolving acid which is an optically active, salt-forming organic acid.
  • Suitable resolving agents for fractional recrystallization methods are, for example, optically active acids, such as the D and L forms of tartaric acid, diacetyltartaric acid, dibenzoyltartaric acid, rnandelic acid, malic acid, lactic acid or the various optically active camphorsulfonic acids such as ⁇ - camphorsulfonic acid.
  • resolving agents suitable for fractional crystallization methods include stereoisomerically pure forms of a-methylbenzylamlne (e.g., S aad R forms, or diastereoisomerically pure forms), 2-phenylglycinol, norephedrine, ephedrine, N- methylephedrme, cyclohexylethylamine, 1, 2-diaminocyclohexane, and the like.
  • stereoisomerically pure forms of a-methylbenzylamlne e.g., S aad R forms, or diastereoisomerically pure forms
  • 2-phenylglycinol norephedrine
  • ephedrine e.g., N- methylephedrme
  • cyclohexylethylamine 1, 2-diaminocyclohexane, and the like.
  • Resolution of racemic mixtures can also be carried out by elution on a column packed with an optically active resolving agent (e.g., dinitrobenzoylphenylglycine).
  • an optically active resolving agent e.g., dinitrobenzoylphenylglycine
  • Suitable elution solvent composition can be determined by one skilled in the art.
  • Tautomeric forms result from the swapping of a single bond with an adjacent double bond together with the concomitant migration of a proton.
  • Tautomeric forms include prototropic tautomers which are isomeric protonation states having the same empirical formula and total charge.
  • Example prototropic tautomers include ketone - enol pairs, amide - imidic acid pairs, lactam - laetim pairs, amide - imidic acid pairs, enamine - imine pairs, and annular forms where a proton can occupy two or more positions of a heterocyclic system, for example, I II- and 3H-imidazole, 1H-, 2H- and 4H- 1, 2, 4-triazole, 1H- and 2H- isoindoie, and 111- and 2H-pyrazole.
  • Tautomeric forms can be in equilibrium or stericaliy locked into one form by appropriate substitution.
  • Compounds of the invention can also include all isotopes of atoms occurring in the intermediates or final compounds.
  • Isotopes include those atoms having the same atomic number but different mass numbers.
  • compound as used herein is meant to include all stereoisomers, geometric isomers, tautomers, and isotopes of the structures depicted.
  • Compounds herein identified by name or structure as one particular tautomeric form are intended to include other tautomeric forms unless otherwise specified (e.g., in the case of purine rings, unless otherwise indicated, when the compound name or structure has the 9H tautomer, it is understood that the 7H tautomer is also encompassed).
  • All compounds, and pharmaceutically acceptable salts thereof, can be found together with other substances such as water and solvents (e.g., hydrates and solvates) or can be isolated.
  • the compounds of the invention, or salts thereof are substantially isolated.
  • substantially isolated is meant that the compound is at least partially or substantially separated from the environment in which it was formed or detected.
  • Partial separation can include, for example, a composition enriched in a compound of the invention.
  • Substantial separation can include compositions containing at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 95%, at least about 97%, or at least about 99% by weight of the compounds of the invention, or salt thereof. Methods for isolating compounds and their salts are routine in the art.
  • phrases "pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
  • ambient temperature and “room temperature,” as used herein, are understood in the art, and refer generally to a temperature, e.g., a reaction temperature, that is about the temperature of the room in which the reaction is carried out, for example, a temperature from about 20 °C to about 30 °C.
  • the present invention also includes pharmaceutically acceptable salts of the compounds described herein.
  • pharmaceutically acceptable salts refers to derivatives of the disclosed compounds wherein the parent compound is modi fied by converting an existing acid or base moiety to its salt form.
  • examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like.
  • the pharmaceutically acceptable salts of the present invention include the conventional non- toxic salts of the parent compound formed, for example, from non-toxic inorganic or organic acids.
  • the pharmaceutically acceptable salts of the present invention can be synthesized from the parent compound which contains a basic or acidic moiety by conventional chemical methods.
  • such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, non-aqueous media like ether, ethyl acetate, alcohols (e.g., methanol, ethanol, iso-propanol, or butanoi) or acetonitrile (MeCN) are preferred.
  • non-aqueous media like ether, ethyl acetate, alcohols (e.g., methanol, ethanol, iso-propanol, or butanoi) or acetonitrile (MeCN) are preferred.
  • non-aqueous media like ether, ethyl acetate, alcohols (e.g., methanol, ethanol, iso-propanol, or butanoi) or acetonitrile (MeCN) are preferred.
  • MeCN acetonitrile
  • the reactions for preparing compounds of the invention can be carried out in suitable solvents which can be readily selected by one of skill in the art of organic synthesis.
  • suitable solvents can be substantially non-reactive with the starting materials (reactants), the intermediates, or products at the temperatures at which the reactions are carried out, e.g. , temperatures which can range from the solvent's freezing temperature to the solvent's boiling temperature.
  • a given reaction can be carried out in one solvent or a mixture of more than one solvent.
  • suitable solvents for a particular reaction step can be selected by the skilled artisan.
  • Reactions can be monitored according to any suitable method known in the art.
  • product formation can be monitored by spectroscopic means, such as nuclear magnetic resonance spectroscopy (e.g. , ! H or C), infrared spectroscopy, spectrophotometry (e.g., UV-visible), mass spectrometry, or by chromatographic methods such as high performance liquid chromatography (HPLC), liquid chromatography-mass spectroscopy (LCMS), or thin layer chromatography (TLC).
  • HPLC high performance liquid chromatography
  • LCMS liquid chromatography-mass spectroscopy
  • TLC thin layer chromatography
  • Compounds can be purified by those skilled in the art by a v ariety of methods, including high performance liquid chromatography (HPLC) ( "Preparative LC-MS Purification: Improved Compound Specific Method Optimization. " Karl F. Blom, Brian Glass, Richard Sparks, Andrew P. Combs J. Combi. Chem. 2004, 6(6), 874- 883
  • Compounds of formula 3b can be prepared by the methods outlined in Scheme 3 starting from compounds of formula 1 and compound 9 by reductive animation in a suitable solvent such as DCM or THF using a reducing agent such as, but not limited to, sodium triacetoxyborohydride, optionally in the presence of an acid such as acetic acid. If any functional groups in compound 1 or 9 are protected to avoid any side reactions, a subsequent deprotection step can be performed to obtain the final product of formula 3b.
  • Cyclopropylamine derivatives of formula J cars be prepared using methods outlined Scheme 4, starting from the ⁇ , ⁇ -unsarurated esters of formula 10 (where R is alkyl such as ethyl) which are either commercially available or prepared using methods disclosed in the literature or detailed herein. Cyclopropanation of compound 10 under standard conditions such as Corey-Chaykovsky reaction can give the cyclopropyl derivatives of formula 11. Tht ester can be saponified to give acids of formula 12, which can be subjected to standard Curtius rearrangement conditions followed by deprotection to give cyclopropylamine derivatives of formula 1.
  • LSDl inhibitors are LSDl inhibitors and. thus, are useful in treating diseases and disorders associated with activity of LSDl .
  • any of the compounds of the invention including any of the embodiments thereof, may be used.
  • the compounds of the invention are selective for LSDl over LSD2, meaning that the compounds bind to or inhibit LSDl with greater affinity or potency, compared to LSD2.
  • selectivity can be at least about 5 -fold, at least about 10-fold, at least about 20-fold, at least about 50-fold, at least about 100-fold, at least about 200-fold, at least about 500-fold or at least about 1000-fold.
  • the compounds of the invention can therefore be used to treat or lessen the se verity of diseases and conditions where LSDl is known to play a role.
  • Diseases and conditions treatable using the compounds of the invention include generally cancers, inflammation, autoimmune diseases, viral induced pathogenesis, he m oglobinopathies, and other diseases linked to LSD 1 activity.
  • Cancers treatable using compounds according to the present invention include, for example, hematological cancers, sarcomas, lung cancers, gastrointestinal cancers, genitourinary tract cancers, liver cancers, bone cancers, nervous system cancers,
  • AML acute myelogenous leukemia
  • APL acute promyelocyte leukemia
  • CLL chronic lymphocytic leukemia
  • Hodgkin lymphoma including relapsed or refractory NHL and recurrent follicular
  • Hodgkin lymphoma including myeloproliferative diseases (e.g., primary myelofibrosis (PMF), polycythemia vera (PV), essential thrombocytosis (ET)), myelodysplasia syndrome (MDS), and multiple myeloma.
  • PMF primary myelofibrosis
  • PV polycythemia vera
  • ET essential thrombocytosis
  • MDS myelodysplasia syndrome
  • Example sarcomas include, for example, chondrosarcoma, Ewing's sarcoma, osteosarcoma, rhabdomyosarcoma, angiosarcoma, fibrosarcoma, liposarcoma, myxoma, rhabdomyoma, fibroma, lipoma, harmatoma, and teratoma.
  • Example lung cancers include, for example, non-small cell lung cancer (NSCLC), bronchogenic carcinoma (squamous cell, undifferentiated small ceil, undifferentiated large cell, adenocarcinoma), alveolar (bronchiolar) carcinoma, bronchial adenoma, chondrornatous hamartoma, and mesothelioma.
  • NSCLC non-small cell lung cancer
  • bronchogenic carcinoma squamous cell, undifferentiated small ceil, undifferentiated large cell
  • adenocarcinoma alveolar (bronchiolar) carcinoma
  • bronchial adenoma chondrornatous hamartoma
  • mesothelioma mesothelioma.
  • Example gastrointestinal cancers include, for example, cancers of the esophagus (squamous cell carcinoma, adenocarcinoma, leiomyosarcoma, lymphoma), stomach (carcinoma, lymphoma, leiomyosarcoma), pancreas (ductal adenocarcinoma, insulinoma, glucagonoma, gastrinoma, carcinoid tumors, vipoma), small bowel (adenocarcinoma, lymphoma, carcinoid tumors, Kaposi's sarcoma, leiomyoma, hemangioma, lipoma, neurofibroma, fibroma), large bowel (adenocarcinoma, tubular adenoma, villous adenoma, hamartoma, leiomyoma), and colorectal cancer.
  • Example genitourinary tract cancers include, for example, cancers of the kidney
  • bladder and urethra squamous cell carcinoma, transitional cell carcinoma, adenocarcinoma), prostate (adenocarcinoma, sarcoma), and testis (seminoma, teratoma, embryonal carcinoma, teratocarcinoma, choriocarcinoma, sarcoma, interstitial cell carcinoma, fibroma, fibroadenoma, adenomatoid tumors, lipoma).
  • Example liver cancers include, for example, hepatoma (hepatocellular carcinoma), cholangiocarcinoma, hepatoblastoma, angiosarcoma, hepatocellular adenoma, and hemangioma.
  • hepatoma hepatocellular carcinoma
  • cholangiocarcinoma hepatoblastoma
  • angiosarcoma hepatocellular adenoma
  • hemangioma hemangioma
  • Example bone cancers include, for example, osteogenic sarcoma (osteosarcoma), fibrosarcoma, malignant fibrous histiocytoma, chondrosarcoma, Ewing's sarcoma, malignant lymphoma (reticulum cell sarcoma), multiple myeloma, malignant giant cell tumor chordoma, osteocbronfroma (osteocartilaginous exostoses), benign chondroma,
  • osteogenic sarcoma osteosarcoma
  • fibrosarcoma malignant fibrous histiocytoma
  • chondrosarcoma chondrosarcoma
  • Ewing's sarcoma malignant lymphoma
  • multiple myeloma malignant giant cell tumor chordoma
  • osteocbronfroma osteocartilaginous exostoses
  • Example nervous system cancers include, for example, cancers of the skull (osteoma, hemangioma, granuloma, xanthoma, osteitis deformans), meninges (meningioma, meningiosarcoma, gliomatosis), brain (astrocytoma, meduoblastoma, glioma, ependymoma, germinoma (pinealoma), glioblastoma multiform, oligodendroglioma, schwannoma, retinoblastoma, congenital tumors), and spinal cord (neurofibroma, meningioma, glioma, sarcoma), as well as neuroblastoma and Lhermitte-Duclos disease.
  • skull osteoma, hemangioma, granuloma, xanthoma, osteitis deformans
  • Example gynecological cancers include, for example, cancers of the uterus
  • cervix cervical carcinoma, pre -tumor cervical dysplasia
  • ovaries ovarian carcinoma (serous cystadenocarcinoma, mucinous cystadenocarcinoma, unclassified carcinoma), granulosa-thecal cell tumors, Sertoli-Leydig cell tumors, dysgerminoma, malignant teratoma), vulva (squamous cell carcinoma, intraepithelial carcinoma, adenocarcinoma, fibrosarcoma, melanoma), vagina (clear cell carcinoma, squamous cell carcinoma, botryoid sarcoma (embryonal rhabdomyosarcoma), and fallopian tubes
  • Example skin cancers include, for example, melanoma, basal cell carcinoma, squamous cell carcinoma, Kaposi's sarcoma, moles dysplastie nevi, lipoma, angioma, dermatofibroma, and keloids.
  • the compounds of the invention can further be used to treat cancer types where LSD ! may be overexpressed including, for example, breast, prostate, head and neck, laryngeal, oral, and thyroid cancers (e.g., papillary thyroid carcinoma).
  • the compounds of the invention can farther be used to treat genetic disorders such as
  • Cowden syndrome and Bannayan-Zonana syndrome are Cowden syndrome and Bannayan-Zonana syndrome.
  • the compounds of the invention can further be used to treat viral diseases such as herpes simplex virus (HSV), varicella zoster virus (VZV), human cytomegalovirus, hepatitis B virus (HBV), and adenovirus.
  • viral diseases such as herpes simplex virus (HSV), varicella zoster virus (VZV), human cytomegalovirus, hepatitis B virus (HBV), and adenovirus.
  • the compounds of the invention can further be used to treat beta-globinopathies including, for example, beta-thalassemia and sickle cell anemia.
  • tire term "contacting” refers to the bringing together of indicated moieties in an in vitro system or an in vivo system.
  • "contacting" a LSD 1 protein with a compound of the invention includes the administration of a compound of the present invention to an individual or patient, such as a human, having a LSD 1 protein, as well as, for example, introducing a compound of the invention into a sample containing a cellular or purified preparation containing the LSD 1 protein.
  • the phrase "therapeutically effective amount” refers to the amount of active compound or pharmaceutical agent that elicits the biological or medicinal response that is being sought in a tissue, system, animal, individual or human by a researcher, veterinarian, medical doctor or other clinician.
  • treating refers to inhibiting the disease; for example, inhibiting a disease, condition or disorder in an individual who is experiencing or displaying the pathology or symptomatology of the disease, condition or disorder (i,e. affiliated arresting further development of the pathology and/or symptomatology) or ameliorating the disease; for example, ameliorating a disease, condition or disorder in an individual who is experiencing or displaying the pathology or symptomatology of the disease, condition or disorder (i.e. ,, reversing the pathology and/or symptomatology) such as decreasing the severity of disease.
  • preventing refers to preventing the disease; for example, preventing a disease, condition or disorder in an individual who may be predisposed to the disease, condition or disorder but does not yet experience or display the pathology or symptomatology of the disease.
  • the compounds of the invention can be used in combination treatments where the compound of the invention is administered in conjunction with other treatments such as the administration of one or more additional therapeutic agents.
  • the additional therapeutic agents are typically those which are normally used to treat the particular condition to be treated.
  • the additional therapeutic agents can include, e.g., chemotherapeutics, anti- inflammatory agents, steroids, immunosuppressants, as well as Bcr-Abl, Flt-3, RAF, FAK, JAK, ⁇ , ⁇ 3 ⁇ inhibitors for treatment of LSD I -mediated diseases, disorders or conditions.
  • the one or more additional pharmaceutical agents can be administered to a patient simultaneously or sequentially.
  • the compounds of the invention can be used in combination with a therapeutic agent that targets an epigenetic regulator.
  • epigenetic regulators include the histone lysine methyltransferases, histone arginine methyl transferases, histone demethylases, histone deacetylases, histone acetylases, and DNA methyltransferases.
  • Histone deacetylase inhibitors include, e.g., vorinostat.
  • the compounds of the invention can be used in combination with chemotherapeutic agents, or other anti-proliferative agents.
  • the compounds of the invention can also be used in combination with medical therapy such as surgery or radiotherapy, e.g., gamma- radiation, neutron beam radiotherapy, electron beam radiotherapy, proton therapy, brachytherapy, and systemic radioactive isotopes.
  • chemotherapeutic agents include any of: abarelix, aldesleukin, alemtuzumab, alitretinoin, allopurinol, altretamine, anasirozole, arsenic trioxide, asparaginase, azacitidine, bendamusiine, bevacizumab, bexarotene, bleomycin, bortezombi, bortezomib, busulfan intravenous, busulfan oral, eaiusteronc, capecitabine, carboplatin, carmustinc, cetuximab, chlorambucil, cisplatin, cladribine, clofarabine, cyclophosphamide, cytarabine, dacarbazine, dactinomycin, dalteparin sodium, dasatmib, daunorubicin, decitabine, denileukin, denileukin dif
  • meclorethamine megestrol acetate, melphalan, mercaptopurine, methotrexate, methoxsalen, mitomycin C, mitotane, mitoxantrone, naridrolone pheripropionate.
  • nelarabine nofetumomab, oxaliplatin, paelitaxel, pamidronate, panitum mab, panobinostat, pegaspargase, pegfllgrastim, pemetrexed disodium, pentostatin, pipobroman, plicamycin, procarbazine, quinacrine, rasburicase, rituximab, ruxoliti ib, sorafenib, stxeptozocin, sunitinib, sunitinib maleate, tamoxifen, temozolomide, teniposide, testolactone, thalidomide, thioguanine, thiotepa, topotecan, toremifene, tositumomab, trastuzumab, tretinoin, uracil mustard, vairubicin, vinblastine, vincristine, vin
  • the compounds of the inventio can be used in combination with ruxolitinib.
  • the compounds of the invention can be used in combination with targeted therapies, including JAK kinase inhibitors
  • the compound of the in vention can be administered in combination with a corticosteroid such as triamcinolone,
  • dexamethasone fluocinolone, cortisone, prednisolone, or flumethoione.
  • the compound of the invention can be administered in combination with an immune suppressant such as fluocinolone acetonide (Retisert®), rimexolone (AL-2178, Vexol, Alcon), or cyclosporine (Restasis®).
  • an immune suppressant such as fluocinolone acetonide (Retisert®), rimexolone (AL-2178, Vexol, Alcon), or cyclosporine (Restasis®).
  • the compound of the in vention can be administered in combination with one or more additional agents selected from
  • DehydrexTM (Holies Labs), Civamide (Opko), sodium hyaluronate (Vismed, Lantibio/TRB Chemedia), cyclosporine (ST-603, Sirion Therapeutics), ARGIOI(T) (testosterone, Argentis), AGR1 G 12(P) (Argentis), ecabet sodium (Senju-Ista), gefarnate (Santen), 15-(s)- hydroxyeicosatetraenoic acid ( 15(S)-HETE), cevilemine, doxycycline (ALTY-0501 , Alacrity), minocycline, iDestrin TM (NP50301, Nascent Pharmaceuticals), cyciosporine A (Nova22007, Novagali), oxytetracyclme (Duramyein, MOLI1901 , Lantibio), CF101 (2S, 3S, 4R, 5R)-3, 4-dihydroxy-5-[6-[(3-iod
  • dehydroepiandrosterone anakinra, efalizumab, mycophenolate sodium, etanercept
  • the compound of the invention can be administered in combination with one or more agents selected from an antibiotic, antiviral, antifungal, anesthetic, anti-inflammatory agents including steroidal and non-steroidal antiinflammatories, and anti-allergic agents.
  • suitable medicaments include aminoglycosides such as amikacin, gentamycin, tobramycin, streptomycin, netilmycin, and kanamycin; fluoroquinolones such as ciprofloxacin, norfloxacin, ofloxacin, trovafloxacin, lomefloxacin, levofloxacin, and enoxacin; naphthyridine; sulfonamides; polymyxin;
  • chloramphenicol neomycin; paramomycin; colistimethate; bacitracin; vancomycin;
  • rifampins tetracyclines
  • rifampins tetracyclines
  • rifampins tetracyclines
  • cycloserine beta-lactams
  • cephalosporins cephalosporins; amphotericins; fluconazole; flucytosine: natamycin; miconazole:
  • ketoconazole corticosteroids; diclofenac; flurbiprofen; ketorolac; suprofen; cromolyn;
  • lodoxamide lodoxamide; levocabastin; naphazoline; antazoline; pheniramine; or azalide antibiotic.
  • agents one or more of which a provided compound may also be combined with include: a treatment for Alzheimer's Disease such as donepezil and rivastigmine; a treatment for Parkinson's Disease such as L-DOPA/carbidopa, entacapone, ropinirole, pramipexole, bromocriptine, pergolide, trihexyphenidyl, and amantadine; an agent for treating multiple sclerosis (MS) such as beta interferon (e.g., Avonex® and Rebif®), glatiramer acetate, and mitoxantrone; a treatment for asthma such as albuterol and montelukast; an agent for treating schizophrenia such as zyprexa, risperdal, seroquel, and haloperidol; an anti- inflammatory agent such as a corticosteroid, such as dexamethasone or prednisone, a TNF blocker, IL-1 RA, aza
  • a neurotrophic factor such as an acetylcholinesterase inhibitor, an MAO inhibitor, an interferon, an anti-corivulsa t, an ion channel blocker, riluzole, or an anti-Parkinson's agent
  • an agent for treating cardiovascular disease such as a beta-blocker, an ACE inhibitor, a diuretic, a nitrate, a calcium channel blocker, or a statin
  • an agent for treating liver disease such as a corticosteroid,
  • cholestyramine an interferon, and an anti- viral agent
  • an agent for treating blood disorders such as a corticosteroid, an anti -leukemic agent, or a growth factor
  • an agent for treating immunodeficiency disorders such as gamma globulin.
  • Biological drags such as antibodies and cytokines, used as anticancer angents, can be combined wit the compounds of the invention, in addition, drags modulating microenvironment or immune responses can be combined wit the compounds of the invention.
  • drags are anti-Her2 antibodies, anti-CD20 antibodies, anti-CTLA l , anti-PD-1, anti-PDLl, and other immunotherapeutic drugs.
  • the compounds of the invention can be administered in the form of pharmaceutical compositions.
  • These compositions can be prepared in a manner well known in the pharmaceutical an, and can be administered by a variety of routes, depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration may be topical (including transdermal, epidermal, ophthalmic and to mucous membranes including intranasal, vaginal and rectal delivery), pulmonary ⁇ e.g., by inhalation or insufflation of powders or aerosols, including by nebulizer; intratracheal or intranasal), oral or parenteral.
  • Parenteral administration includes intravenous, intraarterial, subcutaneous, intraperitoneal intramuscular or injection or infusion; or intracranial, e.g. , intrathecal or intraventricular, administration.
  • Parenteral administration can be in the form of a single bolus dose, or may be, for example, by a continuous perfusion pump.
  • Pharmaceutical compositions and formulations for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable.
  • compositions which contain, as the active ingredient, the compo und of the in v ention or a pharmace utically acceptable salt thereof, in combination with one or more pharmaceutically acceptable carriers (excipients).
  • the composition is suitable for topical administration.
  • the active ingredient is typically mixed with an excipient, diluted by an excipient or enclosed within such a carrier in the form of, for example, a capsule, sachet, paper, or other container.
  • the excipient serves as a diluent, it can be a solid, semi-solid, or liquid material, which acts as a vehicle, carrier or medium for the active ingredient.
  • compositions can be in the form of tablets, pills, powders, lozenges, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, aerosols (as a solid or in a liquid medium), ointments containing, for example, up to 10% by weight of the active compound, soft and hard gelatin capsules, suppositories, sterile injectable solutions, and sterile packaged powders.
  • the active compound in preparing a formulation, can be milled to provide the appropriate particle size prior to combining with the other ingredients, if the active compound is substantially insoluble, it can be milled to a particle size of less than 200 mesh. If the active compound is substantially water soluble, the particle size can be adjusted by milling to provide a substantially uniform distribution in the formulation, e.g., about 40 mesh.
  • the compounds of the invention may be milled using known milling procedures such as wet milling to obtain a particle size appropriate for tablet formation and for other formulation types.
  • Finely divided (nanoparticulate) preparations of the compounds of the invention can be prepared by processes known in the art, e.g. , see International App. No. WO 2002/000196.
  • excipients include lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, calcium phosphate, alginates, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water, syrup, and methyl cellulose.
  • the formulations can additionally include: lubricating agents such as talc, magnesium stearate, and mineral oil; wetting agents; emulsifying and suspending agents; preserving agents such as methyl- and propylhydroxy-benzoates; sweetening agents; and flavoring agents.
  • the compositions of the invention can be formulated so as to provide quick, sustained or delayed release of the active ingredient after administration to the patient by employing procedures known in the art.
  • compositions can be formulated in a unit dosage form, each dosage containing from about 5 to about i,000 mg (1 g), more usually about 100 mg to about 500 mg, of the active ingredient.
  • unit dosage forms refers to physically discrete units suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect, in association with a suitable pharmaceutical excipient.
  • the active compound may be effective over a wide dosage range and is generally administered in a pharmaceutically effective amount It will be understood, however, that the amount of the compound actually administered will usually be determined by a physician, according to the relevant circumstances, including the condition to be treated, the chosen route of administration, the actual compound administered, the age, weight, and response of the individual patient, the severity of the patient's symptoms, and the like.
  • the principal active ingredient is mixed with a pharmaceutical excipient to form a solid preformulation composition containing a homogeneous mixture of a compound of the present invention.
  • a solid preformulation composition containing a homogeneous mixture of a compound of the present invention.
  • the active ingredient is typically dispersed evenly throughout the composition so that the composition can be readily subdivided into equally effective unit dosage forms such as tablets, pills and capsules.
  • preformulation is then subdivided into unit dosage forms of the type described above containing from, for example, about 0.1 to about 1000 mg of the active ingredient of the present invention.
  • the tablets or pills of the present invention can be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action.
  • the tablet or pill can comprise an inner dosage and an outer dosage component, the latter being in the form of an envelope over the former.
  • the two components can be separated by an enteric layer which serves to resist disintegration in the stomach and permit the inner component to pass intact into the duodenum or to be delayed in release.
  • enteric layers or coatings such materials including a number of polymeric acids and mixtures of polymeric acids with such materials as shellac, cetyl alcohol, and cellulose acetate.
  • compositions for inhalation or insufflation include solutions and suspensions in pharmaceutically acceptable, aqueous or organic solvents, or mixtures thereof, and powders.
  • the liquid or solid compositions may contain suitable pharmaceutically acceptable excipients as described supra.
  • the compositions are administered by the oral or nasal respiratory route for local or systemic effect.
  • compositions can be nebulized by use of inert gases. Nebulized solutions may be breathed directly from the nebulizing device or the nebulizing device can be attached to a face masks tent, or intermittent positive pressure breathing machine. Solution, suspension, or powder compositions can be administered orally or nasally from devices which deliver the formulation in an appropriate manner,
  • Topical formulations can contain one or more conventional carriers.
  • ointments can contain water and one or more hydrophobic carriers selected from, for example, liquid paraffin, polyoxyethylene alkyl ether, propylene glycol, white vaseline, and the like.
  • Carrier compositions of creams can be based on water in combination with glycerol and one or more other components, e.g., glycerinemonostearate, PEG- glycerinemonostearate and cetylsiearyl alcohol.
  • Gels can be formulated using isopropyl alcohol and water, suitably in combination with other components such as, for example, glycerol, hydroxyethyl cellulose, and the like.
  • topical formulations contain at least about 0.1 , at least about 0.25, at least about 0.5, at least about 1 , at least about 2, or at least about 5 wt % of the compound of the invention.
  • the topical formulations can be suitably packaged in tubes of, for example, 100 g which are optionally associated with instructions for the treatment of the select indication, e.g. , psoriasis or other skin condition.
  • compositions can be administered to a patient already suffering from a disease in an amount sufficient to cure or at least partially arrest the symptoms of the disease and its complications. Effective doses will depend on the disease condition being treated as well as by the judgment of the attending clinician depending upon factors such as the severity of the disease, the age, weight and general condition of the patient, and the like.
  • compositions administered to a patient can be in the form of pharmaceutical compositions described above. These compositions can be sterilized by conventional sterilization techniques, or may be sterile filtered. Aqueous solutions can be packaged for use as is, or lyophilized, the lyophilized preparation being combined with a sterile aqueous carrier prior to administration.
  • the pH of the compound preparations typically will be between 3 and 11 , more preferably from 5 to 9 and most preferably from 7 to 8. It will be understood that use of certain of the foregoing excipients, carriers, or stabilizers will result in the formation of pharmaceutical salts.
  • the therapeutic dosage of a compound of the present invention can vary according to, for example, the particular use for which the treatment is made, the manner of administration of the compound, the health and condition of the patient, and the judgment of the prescribing physician.
  • the compounds of the invention can be provided in an aqueous physiological buffer solution containing about 0.1 to about 10% w/v of the compound for parenteral administration .
  • Some typical dose ranges are from about 1 ⁇ ig/kg to about I g/kg of body weight per day. In some embodiments, the dose range is from about 0.01 mg/kg to about 100 mg/kg of body weight per day.
  • the dosage is likely to depend on such variables as the type and extent of progression of the disease or disorder, the overall health status of the particular patient, the relative biological efficacy of the compound selected, formulation of the excipient, and its route of administration. Effective doses can be extrapolated from dose-response curves derived from in vitro or animal model test systems.
  • compositions of the invention can further include one or more additional pharmaceutical agents such as a chemotherapeutic, steroid, anti-inflammatory compound, or immunosuppressant, examples of which are listed hereinabo ve.
  • additional pharmaceutical agents such as a chemotherapeutic, steroid, anti-inflammatory compound, or immunosuppressant, examples of which are listed hereinabo ve.
  • the compounds of the invention can be provided with or used in combination with a companion diagnostic.
  • a companion diagnostic refers to a diagnostic device useful for determining the safe and effective use of a therapeutic agent.
  • a companion diagnostic may be used to customize dosage of a therapeutic agent for a given subject, identify appropriate subpopulations for treatment, or identify populations who should not receive a particular treatment because of an increased risk of a serious side effect.
  • the companion diagnostic is used to monitor treatment response in a patient, in some embodiments, the companion diagnostic is used to identify a subject that is likely to benefit from a given compound or therapeutic agent. In some embodiments, the companion diagnostic is used to identify a subject having an increased risk of adverse side effects from administration of a therapeutic agent, compared to a reference standard. In some embodiments, the companion diagnostic is an in vitro diagnostic or imaging tool selected from the list of FDA cleared or appro ved companion diagnostic devices. In some embodiments, the companion diagnostic is selected from the list of tests that have been cleared or approved by the Center for Devices and Radiological Health.
  • Another aspect of the present invention relates to labeled compounds of the invention (radio-labeled, fluorescent-labeled, etc.) that would be useful not only in imaging techniques but also in assays, both in vitro and in vivo, for localizing and quantitating LSD I in tissue samples, including human, and for identifying LSD ! ligands by inhibition binding of a labeled compound.
  • the present invention includes LSD 1 assays that contain such labeled compounds.
  • the present invention further includes isotopicaily- labeled compounds of the invention.
  • An “isotopicaily” or “radio-labeled” compound is a compound of the invention where one or more atoms are replaced or substituted by an atom having an atomic mass or mass number different from the atomic mass or mass number typically found in nature (i.e. , naturally occurring).
  • Suitable radionuclides that may be incorporated in compounds of the present invention include but are not limited to 3 H (also written as T for tritium), l l C, B C, !4 C, l3 N, i 5 N, !
  • radionuclide that is incorporated in the instant radio-labeled compounds will depend on the specific application of that radio-labeled compound.
  • a “radio-labeled " or “labeled compound” is a compound that has incorporated at least one radionuclide.
  • the radionuclide is selected from the group consisting of 3 H, l4 C, i25 I, i5 S and 82 Br, In some embodiments, the compound incorporates 1 , 2, or 3 deuterium atoms.
  • the present invention can further include synthetic methods for incorporating radioisotopes into compounds of the in v ention. Synthetic methods for incorporating radio-isotopes into organic compounds are well known in the art, and an ordinary skill in the art will readily recognize the methods applicable for the compounds of invention.
  • a newly synthesized or identified compound i.e., test compound
  • a test compound which is labeled
  • a test compound can be evaluated for its ability to reduce binding of another compound which is known to bind to LSD1 (i.e., standard compound). Accordingly, the ability of a test compound to compete with the standard compound for binding to
  • LSD 1 directly correlates to its binding affinity.
  • the standard compound is labeled and lest compounds are unlabeled. Accordingly, the concentration of the labeled standard compound is monitored in order to evaluate the competition between the standard compound and the test compound, and the relative binding affinity of the test compound is thus ascertained.
  • Preparatory LC-MS purifications of some of the compounds prepared were performed on Waters mass directed fractionation systems.
  • the basic equipment setup, protocols, and control software for the operation of these systems have been described in detail in the literature. See e.g. "Two-Pump At Column Dilution Configuration for Preparative LC-MS", . Blom, J. Combi. Chem., 4, 295 (2002); "Optimizing Preparative LC-MS Configurations and Methods for Parallel Synthesis Purification", K. Blom, R. Sparks, J. Doughty, G. Everlof, T. Haque, A. Combs, J. Combi.
  • Typical preparative reverse- phase high performance liquid chromatography (RP-HPLC) column conditions are as follows: H - 2 purifications: Waters Sunfire 1M Ci g 5 ⁇ particle size.
  • pH - 10 purifications Waters XBridge Ci g 5 ⁇ particle size, 19 x 100 mm column, eluting with mobile phase A: 0.15% NH 4 OH in water and mobile phase B: acetonitrile; the flow rate was 30 mL/minute, the separating gradient was optimized for each compound usinj the Compound Specific Method Optimization protocol as described in the literature [See “Preparative LCMS Purification: Improved Compound Specific Method Optimization", K. Blom, B. Glass, R. Sparks, A. Combs, J. Comb. Chem. , 6, 874-883 (2004)]. Typically, the flow rate used with 30 x 100 mm column was 60 mL/minute.
  • Step 1 [1- ⁇ ((4-oxopiperidin-i-yl)cyclobutyl] acetonitrile
  • Step I tert- butyl 3-(cyanomethyl)-3- -oxopiperidin-l-yl)azetidine-]-carboxylate
  • Step 2 tert-butyl 3-(cyanomethyl) ⁇ 3 ⁇ 4 ⁇ [(tra -2 ⁇ henylcyclopropyl)amino]piperidin ⁇ l- yl ⁇ azetidine-l-carboxylate
  • Step 3 tert-butyl 3-(cyanomethyl)-3-f4-f(trans-2- phenylcyclopropyl)(Mfluoroacetyl)amino]piperidm-l-yl ⁇ azetidine-l-carboxylate
  • Step 4 N- ⁇ l-[3-(cyanomethyl)azetidm-3-yl]pipetidm-4 ⁇ yl ⁇ -2,2,2-tfifluo
  • Step 5 N-- ⁇ l--[3--(cyanom.e .hyl)- i--methylaze idm ⁇
  • N-(tra;Lv-2-plienylcyclopropyl)aceiamide 24 mg, 0.059 mmol, prepared as described in Example 2, Step 4 ⁇ in DCM (2 mL) was added benzaidehvde (30 ⁇ , 0.29 mmol), followed by acetic acid (10 ⁇ , 0, 18 mmol). The resulting mixture was stirred at room temperature overnight, then Na(OAc)3BH (38 mg, 0.18 mmol) was added. The reaction mixture was stirred at room temperature for 2 h at which time LC-MS indicated the reaction was complete. The mixture was then neutralized with saturated a?.CCb solution and extracted with DCM. The combined extracts were dried oyer Na 2 S04 then concentrated.
  • N-(/ra3 ⁇ 4s-2-pheriylcyclopropyl)aceiamide (20. mg, 0.049 mmol, prepared as described in Example 2, Step 4) in THF (1.0 mL) was added DIEA (43 ⁇ , 0.25 mmol), followed by methanesulfonyl chloride (7.6 , uL, 0.098 mmol). The resulting mixture was stirred at room temperature for 1.5 h then MeOFi (1.0 mL) was added, followed by 2.0 M sodium hydroxide in water (0.12 mL, 0.25 mmol). The reaction mixture was stirred at room temperature for 2 h then diluted with acetonitrile and purified b prep.
  • Example 10 with 3-cyano-4-f1uorobenzoic acid replacing 2-fluoromcotinonitrile.
  • Example 10 with 2-fluorobenzonitrile replacing 2-fluoronicotinonitrile.
  • Example 13
  • Step J tert-butyl 3- ⁇ [(trans-2-phenylcyclopropylJamino]methyl ⁇ azeHdine-l-carboxylate
  • Step 3 allyl (azeUdin-3-ylmethyl)(trans-2-phenylcyclopropyl)carhamate
  • Step 5 [l-(3- ⁇ [(tram-2 ⁇ henylcyclopropyl)amino]methyi ⁇ azetidin-l- yl)cyclobutyl] acetonitrile
  • Step 1 tert-butyl 3- ⁇ [(tra -2 ⁇ henylcyclopropyl)(tnfluoroacetyl)amino]methyl ⁇ azetidine-l- carboxylate
  • Step 3 tert-butyl 4 ⁇ (cyanomethyl)-4-(3 ⁇ [(trans ⁇ 2 ⁇ phenyIcyclopropyI)(tfifluoroace tyl)amino]methyl ⁇ azetidm-l-yl)piperidine-l-carboxylate
  • Step 4 N-( ⁇ l-[4-(cyanomethy1)piperidm-4-yl]azetidm-3-yl ⁇ methyl)- ⁇
  • Step 1 tert-butyl 3'-(cyanomethyl)-3- ⁇ [(trans-2- phenylcy>clopropyl)(Mfluoroacetyl)amino]methyl ⁇ -l,3'-biazeUdine-l '-carboxylate
  • Step 2 (3 ⁇ [(tr ns ⁇ 2-PhenylcycIopropyl)amimijmetfy
  • Step 1 ⁇ l-(Ethyhulfonyl)-3-[4-(hydroxymethyl)piperidin-l-yl]azetidm ⁇
  • Step 2 [l ⁇ (Ethyls lfonyi)-3-(4-fo -3-yl]acetom
  • Step 3 [J-(4- ⁇ [(trans-2-Phenylcyclopropyl)amino]methyl ⁇ piperidin-J- yl)cyclobittyl] acetonitrile
  • Step J tert-Butyl 4 ⁇ -carboxylate
  • Step 2 tert-Butyl 4- ⁇ [[(allyloxy)carhonyl](trans-2- phenylcyclopropyl)amino]methy
  • Step 6 f 3-(4- ⁇ [ ( tra -2-Phenylcyclop pyl)amino]methyJ ⁇ piperidin-l-yJ)azetidin-3- yl] acetonitrile
  • Step 1 Ally! ( ⁇ l-[3-(cyanomethyl)-l-(3-cyanopyridin- yl ⁇ methyl)(trans-2-phenylcyclopropyl)carbamate
  • Step 2 2-[3-(Cy nomet yl)-3-(4- ⁇ [(trans-2 ⁇ enylcyclopropyl)amino] et yl ⁇ pipendin-J- yl)a ⁇ etidin-l-yl]nicotinonitrile
  • Step I tert-Biityl 3-(2-tert ⁇ biitoxy ⁇ 2 ⁇ oxoethylidene)azeUdine ⁇ 1 -carboxylate
  • tert-hutyl (diethoxyphospboryl)acetate (Aldrich, cat#348333: 1.1 g, 4.6 mmol) in THF (15 mL) at 0 °C was added 1.0 M potassium tert-butoxide in THF (4.6 mL, 4.6 mmol). The resulting mixture was warmed to room temperature and stirred for 30 min. The reaction mixture was cooled to 0 °C then a solution of tert-butyl 3-oxoazetidinc-l - carboxylate (Aldrich, catM96315: 0.6 g, 4 mmol) in THF (5 mL) was added.
  • Step 2 tert-Butyl 3-(4- ⁇ [ [ (allyloxy)carbonyl] '(trans-2- phenylcyclopropyi)ammo]methyI ⁇ prperidm
  • Step 3 [3-(4- ⁇ [(irans-2 ⁇ henylcy opropyl)amrno] methyl ⁇ pw
  • Tetrakis(triphenylphosphine)palladiuiTi(0) (8.5 mg) was added to a mixture of tert- butyl 3-(4- ⁇ [[(allyloxy)carbony1](/r /is-2-phenylcyclopropyl)amino
  • Step 1 [3-(4- ⁇ [[(Allyloxy)carbonyl](ira -2 ⁇ henylcyclopropyl)ammo]methyl ⁇ pipen yl)-l-(tert-butoxycarbonyl)aze
  • Step 2 tert-Butyl 3 ⁇ (4 ⁇ (( (allyloxycarbonyl)(trans-2- phenylcyclopropyl)amtno)meih ⁇ )piperidm ⁇
  • reaction mixture was slowly warmed to -40 °C and stirred for 1 h.
  • the mixture was then cooled to -78 °C and a-bromo-4-fluorotoluene (4.9 mL, 40. mmol) was added.
  • the reaction mixture was stirred at - 78 °C for 1 h then quenched with saturated NlLtCi, warmed to room temperature and diluted with ethyl ether.
  • the mixture was then washed with water, brine, dried over Na 2 S04, filtered and
  • Step 2 tert-butyl 4-(4-fluorobenzy -4-(hydroxymethyl)piperidine-l-carboxylate
  • reaction mixture was stirred at room temperature for 5 h then diluted with methylene chloride, washed with 1 N NaOH aqueous solution, water and brine. The organic layer was dried oyer Na2Si filtered and concentrated. The residue was purified by flash
  • Trif!uoroacetic anhydride (2.08 mL, 14.7 mmol) was added to a solution of tert-butyl 4-(4-fluorobenzyl)-4-( ⁇ [(lR,2S)-2-phenylcyclopropyl]amino ⁇ methyl)piperid ne-l- carboxylate (4.3 g, 9.8 mmol) and ⁇ , ⁇ -diisopropylethylamine (4.3 mL, 24 mmol) in methylene chloride (40 mL) at 0 °C. The resulting mixture was stirred at 0 °C for I h then diluted with ether and washed with 1 N HQ, water and brine.
  • Step 7 tert-butyl cyclobutylideneacetat
  • Step 8 tert-butyl [l-(4-(4-fluorobenzyl)-4- ⁇ [[(lR,2S)-2- pheriylcyclopropyl](trifliio
  • Step 9 ⁇ l-[4-(4-fluorobenzyl)-4-( ⁇ [(lR,2S)-2-ph nylcychprop ⁇
  • Trifluoroaeetic acid (0.5 ml.) was added to a solution of tert-butyl [ 1 -(4-(4 ⁇ fiuorohenzyl)-4- ⁇ [[(rR,2S)-2-phenyleyd ⁇
  • Step 1 1-tert-butyl -methyl 4-(methoxymethyl)piperidine-l,4-dicarboxylate
  • Step 2 tert-butyl 4-(hydroxymethyl)-4-(methoxymethyl)piperidine-l-carboxylate
  • Step 5 tert-butyl 4-(methoxymethyl)-4- ⁇ [[(lR,2S)-2-phenylcyclopropyl]- (trifluoroacetyl)amino ] methyljpiperidine- 1 -carboxylate
  • Trif!uoroacetic anhydride (0.96 mL, 6.8 mmol) was added to a solution of tert-butyl 4-(meihoxymethy1)-4-( ⁇ r(l R,2S)-2-phenylcyclopropyl]amin
  • Step 6 2 -trifluoro-N-f[4 ⁇ iethoxymethyl)piperidin-4-yl]methyl ⁇ -N-[(IR S)-2- phenylcyclopropyljaceta ide
  • Step 7 methyl [1 -(4-(methoxymethyl)-4- ⁇ [[ (lR,2S)-2- phenylcyclopropyl] ' (triflno cyclobntyl] acetate
  • Step 8 ⁇ l-[4-(methoxymethyl)-4-( ⁇ [(lR,2S)-2-ph yhyclopropyl]amir ⁇
  • Step 1 tert-btityl 4-methyl-4-( ⁇ [(lR,2S)-2 ⁇ henylcyclopropyl]amino ⁇ methyl)piperidin carboxylate
  • Step 2 tert-butyl 4-methyl-4- ⁇ [[(lR,2S)-2 ⁇ hmylcyclopropyl](Mfluoroacetyl)amino]methyl ⁇ - piperidine- 1 -carboxylate
  • Trifluoroacetic anhydride (0.96 mL, 6.8 mmol) was added to a solution of tert-butyl 4-methyl-4-( ⁇ [(lR,2S)-2-phenyIcyclopropyl]amino ⁇ methyl)piperidme-l -carboxylate (1 ,6 g, 4.5 mmol) and N,N ⁇ diisopropylethylamine (1.6 mL, 9.1 mmol) in methylene chloride (25 mL) at 0 °C. The resulting mixture was stirred at room temperature for i h then diluted with methylene chloride, washed with saturated NaHCCb, water and brine. The organic layer was dried oyer NaiSOa, filtered and concentrated. The residue was purified via flash
  • Step 3 2, 2, 2-tnfluoro-N-[(4-methylpiperidin-4-yl)methyl]-N-[(lR, 2S)-2-phenylcyclopropyl]- acetamide
  • Step 4 tert-butyl [l-(4-methyJ-4- ⁇ [[(lR,2S)-2 ⁇ henylcyclopropyl](tnfluoroacetyl)amino]- methyl ⁇ piperidin-l-yl)cyclo
  • Step 5 ⁇ !-[ 4 ⁇ methyl ⁇ 4 ⁇ ( ⁇ [ (IR,2S)-2-phenylcyclopropyl]amino ⁇ methyl)piperidin- 1- yl]cycIobutyl ⁇ acetic acid
  • Step 1 tert-butyl 3-(cyanomethyl)-3- -oxopiperidin-l-yI)azetidine-l-carboxylate
  • Step 2 tert-butyl 3-(cyanomethyl)-3-(4- ⁇ [ (IR,2S)-2-phenylcyclopropylJamino ⁇ piperidin- 1- yl)azetidine-l-carboxylate
  • Step 4 N- ⁇ l-[3-(cyanomeihyi)a ⁇ eiidin-3-y ⁇
  • Step 5 N- ⁇ l-[3-(cyanomethyl)-l-(methylsuJfonyl)azetidin-3-yl]piperidin ⁇
  • Step 6 [l-(methyhulfonyl)-3-(4- ⁇ [(lR,2S)-2 ⁇ henylcyclopropyl]amino ⁇ piperidm-l- yl)azetidin-3-yI]acetomtrile
  • the reaction mixture was stirred at room temperature overnight then neutralized with saturated Na 2 C03 aqueous solution and extracted with DCM. The combined extracts were dried over Na 2 S0 4 then concentrated. The residue was dissolved in tetrahydrofuran (2 mL) and methanol (2 mL) then 2.0 M sodium hydroxide in water (0.31 mL, 0.62 mmol) was added. The resulting mixture was stirred at 30 °C for 5 h then cooled to room temperature and diluted with DCM. The mixture was washed with water and brine. The organic layer was dried over Na 2 S04 then concentrated.
  • Step 1 tert-butyl 3-(2-tert-butoxy-2-oxoethylidene)azetidine-l-carboxylate
  • the reaction mixture was stirred at room temperature for overnight then diluted with ethyl acetate, washed with saturated NaHCOs aqueous solution, water and brine. The organic layer was dried over NasSQ-i, filtered and concentrated. The residue was purified via flash chromatography on a silica gel column eluting with 0 to 20% EtOAc in hexanes to give the desired product (4.46 g, quant).
  • Step 2 tert-butyl 3-(2 ⁇ ten ⁇ biitoxy ⁇ 2 ⁇ oxoethyl) ⁇ 3 ⁇ (4-oxopiperidin-l-yl)azeUdine ⁇ l-carboxylate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Diabetes (AREA)
  • Oncology (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)
  • Peptides Or Proteins (AREA)
EP15707007.9A 2014-02-13 2015-02-12 Cyclopropylamine als lsd1-hemmer Active EP3105226B1 (de)

Priority Applications (6)

Application Number Priority Date Filing Date Title
EP19190056.2A EP3626714A1 (de) 2014-02-13 2015-02-12 Cyclopropylamine als lsd1-inhibitoren
RS20191440A RS59534B1 (sr) 2014-02-13 2015-02-12 Ciklopropilamini kao lsd1 inhibitori
SI201530894T SI3105226T1 (sl) 2014-02-13 2015-02-12 Ciklopropilamini kot zaviralci LSD1
PL15707007T PL3105226T3 (pl) 2014-02-13 2015-02-12 Cyklopropyloaminy jako inhibitory LSD1
MEP-2019-315A ME03580B (de) 2014-02-13 2015-02-12 Cyclopropylamine als lsd1-hemmer
HRP20192033TT HRP20192033T1 (hr) 2014-02-13 2019-11-08 Ciklopropilamini kao lsd1 inhibitori

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201461939458P 2014-02-13 2014-02-13
US201462061258P 2014-10-08 2014-10-08
PCT/US2015/015635 WO2015123424A1 (en) 2014-02-13 2015-02-12 Cyclopropylamines as lsd1 inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
EP19190056.2A Division EP3626714A1 (de) 2014-02-13 2015-02-12 Cyclopropylamine als lsd1-inhibitoren

Publications (2)

Publication Number Publication Date
EP3105226A1 true EP3105226A1 (de) 2016-12-21
EP3105226B1 EP3105226B1 (de) 2019-09-04

Family

ID=52595463

Family Applications (2)

Application Number Title Priority Date Filing Date
EP15707007.9A Active EP3105226B1 (de) 2014-02-13 2015-02-12 Cyclopropylamine als lsd1-hemmer
EP19190056.2A Withdrawn EP3626714A1 (de) 2014-02-13 2015-02-12 Cyclopropylamine als lsd1-inhibitoren

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP19190056.2A Withdrawn EP3626714A1 (de) 2014-02-13 2015-02-12 Cyclopropylamine als lsd1-inhibitoren

Country Status (33)

Country Link
US (4) US9493450B2 (de)
EP (2) EP3105226B1 (de)
JP (3) JP6602779B2 (de)
KR (1) KR102352408B1 (de)
CN (1) CN106488915B (de)
AU (2) AU2015217119C1 (de)
BR (1) BR112016018555B1 (de)
CA (1) CA2939081C (de)
CL (1) CL2016002021A1 (de)
CR (2) CR20200362A (de)
CY (1) CY1122314T1 (de)
DK (1) DK3105226T3 (de)
EA (1) EA201691594A1 (de)
EC (1) ECSP16073171A (de)
ES (1) ES2750956T3 (de)
HR (1) HRP20192033T1 (de)
HU (1) HUE045725T2 (de)
IL (2) IL246950B (de)
LT (1) LT3105226T (de)
ME (1) ME03580B (de)
MX (2) MX2016010390A (de)
MY (1) MY196877A (de)
NZ (1) NZ723203A (de)
PE (1) PE20161384A1 (de)
PH (1) PH12016501546A1 (de)
PL (1) PL3105226T3 (de)
PT (1) PT3105226T (de)
RS (1) RS59534B1 (de)
SG (2) SG10201806846RA (de)
SI (1) SI3105226T1 (de)
TW (2) TWI664164B (de)
UA (1) UA122389C2 (de)
WO (1) WO2015123424A1 (de)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9428470B2 (en) 2014-02-13 2016-08-30 Takeda Pharmaceutical Company Limited Heterocyclic compound
TWI664164B (zh) 2014-02-13 2019-07-01 美商英塞特控股公司 作為ｌｓｄ１抑制劑之環丙胺
US9346776B2 (en) 2014-02-13 2016-05-24 Takeda Pharmaceutical Company Limited Fused heterocyclic compound
WO2015123408A1 (en) 2014-02-13 2015-08-20 Incyte Corporation Cyclopropylamines as lsd1 inhibitors
JP6602778B2 (ja) 2014-02-13 2019-11-06 インサイト・コーポレイション Ｌｓｄ１阻害剤としてのシクロプロピルアミン類
US9527835B2 (en) 2014-02-13 2016-12-27 Incyte Corporation Cyclopropylamines as LSD1 inhibitors
WO2016007727A1 (en) 2014-07-10 2016-01-14 Incyte Corporation Triazolopyridines and triazolopyrazines as lsd1 inhibitors
TW201613925A (en) 2014-07-10 2016-04-16 Incyte Corp Imidazopyrazines as LSD1 inhibitors
US9695167B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors
TWI687419B (zh) 2014-07-10 2020-03-11 美商英塞特公司 作為ｌｓｄ１抑制劑之咪唑并吡啶及咪唑并吡嗪
SG11201708047UA (en) 2015-04-03 2017-10-30 Incyte Corp Heterocyclic compounds as lsd1 inhibitors
KR20180011331A (ko) 2015-06-12 2018-01-31 오리존 지노믹스 에스.에이. Lsd1 억제제와 관련된 바이오마커 및 그의 용도
WO2017013061A1 (en) 2015-07-17 2017-01-26 Oryzon Genomics, S.A. Biomarkers associated with lsd1 inhibitors and uses thereof
EP3334709A1 (de) 2015-08-12 2018-06-20 Incyte Corporation Salze eines lsd1-hemmers
WO2017079476A1 (en) 2015-11-05 2017-05-11 Mirati Therapeutics, Inc. Lsd1 inhibitors
AU2016382463B2 (en) 2015-12-29 2021-05-27 Mirati Therapeutics, Inc. LSD1 inhibitors
BR112018068565A2 (pt) 2016-03-15 2019-02-12 Oryzon Genomics, S.A. combinações de inibidores de lsd1 para uso no tratamento de tumores sólidos
WO2017158136A1 (en) 2016-03-16 2017-09-21 Oryzon Genomics, S.A. Methods to determine kdm1a target engagement and chemoprobes useful therefor
CN107200706A (zh) * 2016-03-16 2017-09-26 中国科学院上海药物研究所 一类氟取代的环丙胺类化合物及其制备方法、药物组合物和用途
WO2017184934A1 (en) 2016-04-22 2017-10-26 Incyte Corporation Formulations of an lsd1 inhibitor
CN107459476B (zh) * 2016-06-03 2022-06-24 中国科学院上海药物研究所 反吲哚啉环丙胺类化合物及其制备方法、药物组合物和用途
US20190256929A1 (en) 2016-11-03 2019-08-22 Oryzon Genomics, S.A. Pharmacodynamic biomarkers for personalized cancer care using epigenetic modifying agents
EP3535420A1 (de) 2016-11-03 2019-09-11 Oryzon Genomics, S.A. Biomarker zur bestimmung der ansprechempfindlichkeit auf lsd1-inhibitoren
JP7352284B2 (ja) 2017-05-15 2023-09-28 ザ・リージェンツ・オブ・ザ・ユニバーシティ・オブ・ミシガン ＬＳＤ－１インヒビターとしてのピロロ〔２，３－ｃ〕ピリジン及び関連類似体
CA3071804A1 (en) 2017-08-03 2019-02-07 Oryzon Genomics, S.A. Methods of treating behavior alterations
WO2019068326A1 (en) 2017-10-05 2019-04-11 Université D'aix-Marseille INHIBITORS OF LSD1 FOR THE TREATMENT AND PREVENTION OF CARDIOMYOPATHIES
WO2019222069A1 (en) 2018-05-15 2019-11-21 The Regents Of The University Of Michigan Imidazo[4,5-c]pyridine compounds as lsd-1 inhibitors
US10968200B2 (en) 2018-08-31 2021-04-06 Incyte Corporation Salts of an LSD1 inhibitor and processes for preparing the same
WO2020113094A1 (en) 2018-11-30 2020-06-04 Nuvation Bio Inc. Pyrrole and pyrazole compounds and methods of use thereof
WO2020188089A1 (en) 2019-03-20 2020-09-24 Oryzon Genomics, S.A. Methods of treating attention deficit hyperactivity disorder using kdm1a inhibitors such as the compound vafidemstat
SG11202109159VA (en) 2019-03-20 2021-10-28 Oryzon Genomics Sa Methods of treating borderline personality disorder
CN114341366A (zh) 2019-07-05 2022-04-12 奥莱松基因组股份有限公司 用于使用kdm1a抑制剂个体化治疗小细胞肺癌的生物标志物和方法
EP3964204A1 (de) 2020-09-08 2022-03-09 Université d'Aix-Marseille Verbindungen zur verwendung bei der behandlung und vorbeugung von gewebefibrose
KR20230167102A (ko) 2021-04-08 2023-12-07 오리존 지노믹스 에스.에이. 골수성 암 치료를 위한 lsd1 억제제의 조합물
WO2023217784A1 (en) 2022-05-09 2023-11-16 Oryzon Genomics, S.A. Methods of treating nf1-mutant tumors using lsd1 inhibitors
WO2023217758A1 (en) 2022-05-09 2023-11-16 Oryzon Genomics, S.A. Methods of treating malignant peripheral nerve sheath tumor (mpnst) using lsd1 inhibitors
WO2024110649A1 (en) 2022-11-24 2024-05-30 Oryzon Genomics, S.A. Combinations of lsd1 inhibitors and menin inhibitors for treating cancer

Family Cites Families (316)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL7013068A (de) 1969-09-17 1971-03-19
US4537889A (en) 1982-12-27 1985-08-27 Eli Lilly And Company Inotropic agents
US4614810A (en) 1984-09-24 1986-09-30 Pennwalt Corporation 4,5-dihydro-4-oxo-2-[(2-trans-phenylcyclopropyl)amino]-3-furancarboxylic acids and derivatives thereof
US4625040A (en) 1984-09-24 1986-11-25 Pennwalt Corporation N-(phenyl) or N-(phenylcyclopropyl)-2,5-dihydro-2-oxo-4[(substituted phenyl)amino]-3-furancarboxamide derivatives
FR2607813B1 (fr) 1986-12-05 1989-03-31 Montpellier I Universite Alkylamino-8 imidazo (1,2-a) pyrazines et derives, leur preparation et leur application en therapeutique
JPH032778Y2 (de) 1986-12-15 1991-01-24
AU622330B2 (en) 1989-06-23 1992-04-02 Takeda Chemical Industries Ltd. Condensed heterocyclic compounds having a nitrogen atom in the bridgehead for use as fungicides
JP2844351B2 (ja) 1989-07-13 1999-01-06 株式会社科薬 安定なポリミキシン系抗生物質水性溶液
IL96432A0 (en) 1989-11-30 1991-08-16 Schering Ag Pesticidal compositions containing pyridine derivatives and novel pyridine derivatives
FR2662163A1 (fr) 1990-05-16 1991-11-22 Lipha Nouvelles 8-amino-1,2,4-triazolo(4,3-a) pyrazines, procedes de preparation et medicaments les contenant.
AU4293393A (en) 1992-06-17 1994-01-04 Upjohn Company, The Pyridino-, pyrrolidino- and azepino-substituted oximes useful as anti-atherosclerosis and anti-hypercholesterolemic agents
JP2923139B2 (ja) 1992-10-05 1999-07-26 三井化学株式会社 製 剤
DE4327027A1 (de) 1993-02-15 1994-08-18 Bayer Ag Imidazoazine
FR2711993B1 (fr) 1993-11-05 1995-12-01 Rhone Poulenc Rorer Sa Médicaments contenant des dérivés de 7H-imidazol[1,2-a]pyrazine-8-one, les nouveaux composés et leur préparation.
US5932223A (en) 1996-09-26 1999-08-03 Merck & Co., Inc. Rotavirus vaccine formulations
BR9814628A (pt) 1997-11-11 2001-11-27 Ono Pharmaceutical Co Derivados de pirazina fundidos
JP2000319278A (ja) 1999-05-11 2000-11-21 Ono Pharmaceut Co Ltd 縮合ピラジン化合物およびその化合物を有効成分とする薬剤
JP2000319277A (ja) 1999-05-11 2000-11-21 Ono Pharmaceut Co Ltd 縮合ピラジン化合物およびその化合物を有効成分とする薬剤
JP4032566B2 (ja) 1999-06-21 2008-01-16 東レ株式会社 発光素子
JP4041624B2 (ja) 1999-07-21 2008-01-30 三井化学株式会社 有機電界発光素子
JP2001057292A (ja) 1999-08-20 2001-02-27 Toray Ind Inc 発光素子
NZ518052A (en) 1999-09-28 2005-04-29 Panacea Biotec Ltd Controlled release compositions comprising nimesulide (4-nitro-2-phenoxymethanesulfonanilide) for a once-a-day oral dosage to treat diseases such as arthritis
SE9903611D0 (sv) 1999-10-06 1999-10-06 Astra Ab Novel compounds III
DE19948434A1 (de) 1999-10-08 2001-06-07 Gruenenthal Gmbh Substanzbibliothek enthaltend bicyclische Imidazo-5-amine und/oder bicyclische Imidazo-3-amine
JP4409680B2 (ja) 1999-10-18 2010-02-03 株式会社ヤクルト本社 三環性縮合イミダゾール誘導体
DK1277754T3 (da) 2000-04-27 2005-11-14 Astellas Pharma Inc Imidazopyridinderivater
US6403588B1 (en) 2000-04-27 2002-06-11 Yamanouchi Pharmaceutical Co., Ltd. Imidazopyridine derivatives
AU1560802A (en) 2000-06-28 2002-01-08 Smithkline Beecham Plc Wet milling process
AR029538A1 (es) 2000-07-06 2003-07-02 Wyeth Corp Composiciones farmaceuticas de agentes estrogenicos
WO2002006286A2 (en) 2000-07-14 2002-01-24 Bristol-Myers Squibb Pharma Company IMIDAZO[1,2-a]PYRAZINES FOR THE TREATMENT OF NEUROLOGICAL DISORDERS
DE10050663A1 (de) 2000-10-13 2002-04-18 Gruenenthal Gmbh Verwendung von substituierten Imidazo[1,2-a]pyridin-, -pyrimidin- und pyrazin-3-yl-amin-Derivaten zur Herstellung von Medikamenten zur NOS-Inhibierung
AU2001295992A1 (en) 2000-10-24 2002-05-06 Sankyo Company Limited Imidazopyridine derivatives
JP2002205992A (ja) 2000-11-08 2002-07-23 Takeda Chem Ind Ltd 二環式トリアゾロン誘導体およびそれを含有する除草剤
EP1343788B1 (de) 2000-11-10 2005-11-23 MERCK SHARP & DOHME LTD. Imidazotriazin-derivate als liganden für gaba-rezeptoren
AU2002224927A1 (en) 2000-12-13 2002-06-24 Basf Aktiengesellschaft Use of substituted imidazoazines, novel imidazoazines, methods for the production thereof, and agents containing these compounds
EP1217000A1 (de) 2000-12-23 2002-06-26 Aventis Pharma Deutschland GmbH Faktor Xa und Faktor VIIa Inhibitoren
TWI312347B (en) 2001-02-08 2009-07-21 Eisai R&D Man Co Ltd Bicyclic nitrogen-containing condensed ring compounds
US6951848B2 (en) 2001-03-12 2005-10-04 Millennium Pharmaceuticals, Inc., Functionalized heterocycles as modulators of chemokine receptor function and methods of use therefor
AR035543A1 (es) 2001-06-26 2004-06-16 Japan Tobacco Inc Agente terapeutico para la hepatitis c que comprende un compuesto de anillo condensado, compuesto de anillo condensado, composicion farmaceutica que lo comprende, compuestos de benzimidazol, tiazol y bifenilo utiles como intermediarios para producir dichos compuestos, uso del compuesto de anillo con
IL159811A0 (en) 2001-07-13 2004-06-20 Neurogen Corp Heteroaryl substituted fused bicyclic heteroaryl compounds as gabaa receptor ligands
US6921762B2 (en) 2001-11-16 2005-07-26 Amgen Inc. Substituted indolizine-like compounds and methods of use
US20050113283A1 (en) 2002-01-18 2005-05-26 David Solow-Cordero Methods of treating conditions associated with an EDG-4 receptor
AU2003214873A1 (en) 2002-01-18 2003-09-02 Ceretek Llc Methods of treating conditions associated with an edg receptor
WO2004017950A2 (en) 2002-08-22 2004-03-04 Piramed Limited Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents
UA80296C2 (en) 2002-09-06 2007-09-10 Biogen Inc Imidazolopyridines and methods of making and using the same
WO2005014777A2 (en) 2002-10-16 2005-02-17 Board Of Regents, The University Of Texas System Methods and compositions for increasing the efficacy of biologically-active ingredients
JP2006514043A (ja) 2002-12-20 2006-04-27 ファルマシア・コーポレーション マイトジェン活性化タンパク質キナーゼ−活性化タンパク質キナーゼ−２を阻害する化合物
WO2004072080A1 (en) 2003-02-10 2004-08-26 Cellular Genomics, Inc. Certain 8-heteroaryl-6-phenyl-imidazo[1,2-a]pyrazines as modulators of hsp90 complex activity
GB0303910D0 (en) 2003-02-20 2003-03-26 Merck Sharp & Dohme Therapeutic agents
US7157460B2 (en) 2003-02-20 2007-01-02 Sugen Inc. Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
US7186832B2 (en) 2003-02-20 2007-03-06 Sugen Inc. Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
EP2385040A1 (de) 2003-03-14 2011-11-09 ONO Pharmaceutical Co., Ltd. Stickstoffhaltige heterocyclische Derivate und Arzneimittel, die diese als Wirkstoff enthalten
JP2006522750A (ja) 2003-04-11 2006-10-05 ノボ　ノルディスク　アクティーゼルスカブ 代謝性症候群ならびに関連の疾患および障害を治療するために、１１β−ヒドロキシステロイドデヒドロゲナーゼ１型阻害剤および抗高血圧剤を使用する併用療法
DK1615647T3 (da) 2003-04-11 2010-04-06 High Point Pharmaceuticals Llc Farmaceutisk anvendelse af kondenserede 1,2,4-triazoler
ATE512957T1 (de) 2003-04-24 2011-07-15 Merck Sharp & Dohme Hemmer der akt aktivität
SE0301653D0 (sv) 2003-06-05 2003-06-05 Astrazeneca Ab Novel compounds
AU2004257267B2 (en) 2003-07-14 2009-12-03 Arena Pharmaceuticals,Inc Fused-aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto
US7538120B2 (en) 2003-09-03 2009-05-26 Array Biopharma Inc. Method of treating inflammatory diseases
WO2005025558A1 (en) 2003-09-12 2005-03-24 Applied Reserach Systems Ars Holding N.V. Sulfonamide derivatives for the treatment of diabetes
JP2005089352A (ja) 2003-09-16 2005-04-07 Kissei Pharmaceut Co Ltd 新規なイミダゾ［１，５−ａ］ピラジン誘導体、それを含有する医薬組成物およびそれらの用途
CA2541832C (en) 2003-10-10 2009-11-24 Pfizer Products Inc. Substituted 2h-[1,2,4]triazolo[4,3-a]pyrazines as gsk-3 inhibitors
US7419978B2 (en) 2003-10-22 2008-09-02 Bristol-Myers Squibb Company Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors
JP4842829B2 (ja) 2003-10-31 2011-12-21 武田薬品工業株式会社 含窒素縮合複素環化合物
WO2005063241A1 (ja) 2003-12-26 2005-07-14 Ono Pharmaceutical Co., Ltd. ミトコンドリアベンゾジアゼピン受容体介在性疾患の予防および／または治療剤
WO2005077948A1 (ja) 2004-02-16 2005-08-25 Daiichi Pharmaceutical Co., Ltd. 抗真菌作用複素環化合物
US7306631B2 (en) 2004-03-30 2007-12-11 The Procter & Gamble Company Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
EP1756103A2 (de) * 2004-04-26 2007-02-28 Pfizer, Inc. Pyrrolopyridinderivate und deren verwendung als inhibitoren der hiv-integrase
ATE516019T1 (de) 2004-05-11 2011-07-15 Egalet Ltd Quellbare dosierform mit gellan-gummit
WO2006015263A2 (en) 2004-07-29 2006-02-09 Threshold Pharmaceuticals, Inc. Lonidamine analogs
EP1781655A2 (de) 2004-08-18 2007-05-09 Pharmacia & Upjohn Company LLC Triazolopyridinverbindungen zur entzündungsbehandlung
EP1799671A4 (de) 2004-09-02 2009-06-10 Smithkline Beecham Corp Chemische verbindungen
US7524860B2 (en) 2004-10-07 2009-04-28 Pfizer Inc. Antibacterial agents
WO2006057946A2 (en) 2004-11-22 2006-06-01 Threshold Pharmaceuticals, Inc. Tubulin binding anti cancer agents and prodrugs thereof
AU2005311451A1 (en) 2004-12-01 2006-06-08 Merck Serono Sa [1,2,4]triazolo[4,3-a]pyridine derivatives for the treatment of hyperproliferative diseases
WO2007149479A1 (en) 2006-06-22 2007-12-27 Mallinckrodt Inc. Pyrazine derivatives and uses thereof in renal monitoring
US20070293456A9 (en) 2004-12-30 2007-12-20 Anthony Hayford Method for the synthesis of 3-substituted indolizine and benzoindolizine compounds
US7456289B2 (en) 2004-12-31 2008-11-25 National Health Research Institutes Anti-tumor compounds
JP4130220B1 (ja) 2005-02-22 2008-08-06 ファイザー株式会社 ５ｈｔ４受容体アゴニストとしてのオキシインドール誘導体
ITBO20050123A1 (it) 2005-03-07 2005-06-06 Alfa Wassermann Spa Formulazioni farmaceutiche gastroresistenti contenenti rifaximina
WO2006113704A2 (en) 2005-04-18 2006-10-26 Neurogen Corporation Subtituted heteroaryl cb1 antagonists
US7572807B2 (en) 2005-06-09 2009-08-11 Bristol-Myers Squibb Company Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors
US7579360B2 (en) 2005-06-09 2009-08-25 Bristol-Myers Squibb Company Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors
DE602005023544D1 (de) 2005-06-09 2010-10-21 Oncalis Ag Angiogeneseinhibitoren
US7452892B2 (en) 2005-06-17 2008-11-18 Bristol-Myers Squibb Company Triazolopyrimidine cannabinoid receptor 1 antagonists
TW200726765A (en) 2005-06-17 2007-07-16 Bristol Myers Squibb Co Triazolopyridine cannabinoid receptor 1 antagonists
US7632837B2 (en) 2005-06-17 2009-12-15 Bristol-Myers Squibb Company Bicyclic heterocycles as cannabinoid-1 receptor modulators
US7709468B2 (en) 2005-09-02 2010-05-04 Abbott Laboratories Imidazo based heterocycles
ES2349476T3 (es) 2005-09-09 2011-01-03 Schering Corporation Nuevos derivados de 4-ciano, 4-amino y 4-aminometilo de compuestos de pirazolo[1,5-a]piridinas, pirazolo[1,5-c]pirimidinas y 2h-indazol y derivados de 5-ciano, 5-amino y 5-aminometilo de compuestos de imidazo[1,2-a]piridinas e imidazo[1,5-a]pirazinas, como inhibidores de cinasa dependiente de ciclina.
CA2628455A1 (en) 2005-11-10 2007-05-24 Schering Corporation Imidazopyrazines as protein kinase inhibitors
AU2006318349B2 (en) 2005-11-28 2010-08-19 Marinus Pharmaceuticals Ganaxolone formulations and methods for the making and use thereof
AU2006331363B2 (en) 2005-12-27 2012-07-05 F. Hoffmann-La Roche Ag Aryl-isoxazol-4-yl-imidazo[1, 5-a]pyridine derivatives
WO2007074491A1 (en) 2005-12-28 2007-07-05 Universita Degli Studi Di Siena HETEROTRICYCLIC AMIDE DERIVATIVES AS NEUROKININ-l (NKl) RECEPTOR LIGANDS
PE20070978A1 (es) 2006-02-14 2007-11-15 Novartis Ag COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks)
US8097617B2 (en) 2006-03-31 2012-01-17 Novartis Ag Organic compounds
US20090175852A1 (en) 2006-06-06 2009-07-09 Schering Corporation Imidazopyrazines as protein kinase inhibitors
TW200808802A (en) 2006-06-06 2008-02-16 Schering Corp Imidazopyrazines as protein kinase inhibitors
JP2009541323A (ja) 2006-06-22 2009-11-26 マリンクロット インコーポレイテッド 拡張された共役を有するピラジン誘導体およびその使用
CN101506198A (zh) 2006-06-29 2009-08-12 先灵公司 取代的双环和三环凝血酶受体拮抗剂
WO2008005423A1 (en) 2006-07-03 2008-01-10 Cambrex Charles City, Inc. Improved method of making sufentanil
WO2008005908A2 (en) 2006-07-07 2008-01-10 Forest Laboratories Holdings Limited Pyridoimidazole derivatives
US8217177B2 (en) 2006-07-14 2012-07-10 Amgen Inc. Fused heterocyclic derivatives and methods of use
US8198448B2 (en) 2006-07-14 2012-06-12 Amgen Inc. Fused heterocyclic derivatives and methods of use
PE20080403A1 (es) 2006-07-14 2008-04-25 Amgen Inc Derivados heterociclicos fusionados y metodos de uso
AU2007275221A1 (en) 2006-07-20 2008-01-24 Allen J. Borchardt Benzothiophene inhibitors of RHO kinase
WO2008027812A2 (en) 2006-08-28 2008-03-06 Forest Laboratories Holdings Limited Imidazopyridine and imidazopyrimidine derivatives
DE102006041292A1 (de) 2006-09-01 2008-03-06 Henkel Kgaa Wasserstoffperoxid-Aktivierung mit N-Heterocyclen
WO2008037607A1 (de) 2006-09-25 2008-04-03 Basf Se Carbonylgruppen-enthaltende heterocyclische verbindungen und deren verwendung zur bekämpfung von phytopathogenen pilzen
ATE542818T1 (de) 2006-10-11 2012-02-15 Amgen Inc Imidazo- und triazolopyridinverbindungen und verfahren zu deren anwendung
CA2669094A1 (en) 2006-11-08 2008-05-29 Novavax,Inc. Method of preparing solid dosage forms of multi-phasic pharmaceutical compositions
WO2008056176A1 (en) 2006-11-10 2008-05-15 Scottish Biomedical Limited Pyrazolopyrimidines as phosphodiesterase inhibitors
LT3034075T (lt) 2006-11-22 2018-11-26 Incyte Holdings Corporation Imidazotriazinai ir imidazopirimidinai kaip kinazės inhibitoriai
DE602007012133D1 (de) 2006-12-01 2011-03-03 Andrew Burritt Triazolopyridinverbindungen zur behandlung von degenerations- und entzündungskrankheiten
WO2008079404A2 (en) 2006-12-22 2008-07-03 Combinatorx, Incorporated Pharmaceutical compositions for treatment of parkinson's disease and related disorders
WO2008110523A1 (en) 2007-03-09 2008-09-18 Probiodrug Ag Imidazo [1,5-a] pyridine derivatives as inhibitors of glutaminyl cyclase
DE102007012645A1 (de) 2007-03-16 2008-09-18 Bayer Healthcare Ag Substituierte Imidazo- und Triazolopyrimidine
EP1972628A1 (de) 2007-03-21 2008-09-24 Schwarz Pharma Ag Indolizine und aza-analoge Derivate davon als CNS-aktive Verbindungen
CN101679428A (zh) 2007-04-16 2010-03-24 利奥制药有限公司 用于治疗皮肤疾病的作为磷酸二酯酶抑制剂的三唑并吡啶类
WO2008130951A1 (en) 2007-04-17 2008-10-30 Bristol-Myers Squibb Company Fused heterocyclic 11-beta-hydroxysteroid dehydrogenase type i inhibitors
CN101855222A (zh) 2007-05-10 2010-10-06 通用电气健康护理有限公司 对大麻素cb2受体具有活性的咪唑并(1,2-a)吡啶和相关化合物
AU2008254038B2 (en) 2007-05-21 2013-01-10 Toray Industries, Inc. Oral preparation comprising specific organic acid, and method for improvement in elution property and chemical stability of oral preparation
CN101790526A (zh) 2007-06-08 2010-07-28 雅培制药有限公司 用作激酶抑制剂的5-杂芳基取代的吲唑化合物
US8648069B2 (en) 2007-06-08 2014-02-11 Abbvie Inc. 5-substituted indazoles as kinase inhibitors
CN101772500A (zh) 2007-06-14 2010-07-07 先灵公司 作为蛋白质激酶抑制剂的咪唑并吡嗪
CL2008001839A1 (es) 2007-06-21 2009-01-16 Incyte Holdings Corp Compuestos derivados de 2,7-diazaespirociclos, inhibidores de 11-beta hidroxil esteroide deshidrogenasa tipo 1; composicion farmaceutica que comprende a dichos compuestos; utiles para tratar la obesidad, diabetes, intolerancia a la glucosa, diabetes tipo ii, entre otras enfermedades.
US20090004281A1 (en) 2007-06-26 2009-01-01 Biovail Laboratories International S.R.L. Multiparticulate osmotic delivery system
PE20090492A1 (es) 2007-07-18 2009-05-27 Novartis Ag Compuestos heterociclos como inhibidores de cinasa de fosfatidil-inositol-3
MX2010001340A (es) 2007-07-31 2010-06-02 Schering Corp Combianacion de agente antimitotico e inhibidor de aurora quinasa como tratamiento anticancerigeno.
WO2009017954A1 (en) 2007-08-01 2009-02-05 Phenomix Corporation Inhibitors of jak2 kinase
MX2010001650A (es) 2007-08-10 2010-08-02 Glaxosmithkline Llc Entidades quimicas biciclicas que contienen nitrogeno para el tratamiento de infecciones virales.
US20090047336A1 (en) 2007-08-17 2009-02-19 Hong Kong Baptist University novel formulation of dehydrated lipid vesicles for controlled release of active pharmaceutical ingredient via inhalation
FR2920091A1 (fr) 2007-08-24 2009-02-27 Oreal Composition tinctoriale comprenant une base d'oxydation aminopyrazolopyridine, un coupleur et un polyol particulier.
FR2920090A1 (fr) 2007-08-24 2009-02-27 Oreal Composition tinctoriale comprenant une base d'oxydation aminopyrazolopyridine particuliere, un coupleur et un tensioactif particulier.
KR20090022616A (ko) 2007-08-31 2009-03-04 한올제약주식회사 베실산클로피도그렐 함유 경구투여용 약제
US8119658B2 (en) 2007-10-01 2012-02-21 Bristol-Myers Squibb Company Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors
GB0719803D0 (en) 2007-10-10 2007-11-21 Cancer Rec Tech Ltd Therapeutic compounds and their use
CN101861321B (zh) 2007-10-11 2013-02-06 阿斯利康(瑞典)有限公司 作为蛋白激酶b抑制剂的吡咯并[2,3-d]嘧啶衍生物
KR101600098B1 (ko) 2007-10-12 2016-03-04 노파르티스 아게 스핑고신 1 포스페이트 (ｓ1ｐ) 수용체 조절제를 포함하는 조성물
US7820665B2 (en) 2007-12-19 2010-10-26 Amgen Inc. Imidazopyridazine inhibitors of PI3 kinase for cancer treatment
JP5710268B2 (ja) 2007-12-19 2015-04-30 ジェネンテック， インコーポレイテッド ８−アニリノイミダゾピリジン及びその抗ガン及び／又は抗炎症剤としての使用
KR100988233B1 (ko) 2007-12-26 2010-10-18 한미홀딩스 주식회사 클로피도그렐 1,5-나프탈렌 다이술폰산 염 또는 이의수화물의 약학 조성물 및 제제
RS55263B1 (sr) 2008-03-11 2017-02-28 Incyte Holdings Corp Derivati azetidina i ciklobutana kao jak inhibitori
CA2718403A1 (en) 2008-03-13 2009-09-17 The General Hospital Corporation Inhibitors of the bmp signaling pathway
JP5547099B2 (ja) 2008-03-14 2014-07-09 インテリカイン， エルエルシー キナーゼ阻害剤および使用方法
WO2009128520A1 (ja) 2008-04-18 2009-10-22 塩野義製薬株式会社 Ｐ１３ｋ阻害活性を有する複素環化合物
DE102008023801A1 (de) 2008-05-15 2009-11-19 Bayer Schering Pharma Aktiengesellschaft Substituierte Imidazo- und Triazolopyrimidine, Imidazo- und Pyrazolopyrazine und Imidazotriazine
US8349210B2 (en) 2008-06-27 2013-01-08 Transitions Optical, Inc. Mesogenic stabilizers
WO2010010187A1 (en) 2008-07-25 2010-01-28 Galapagos Nv Novel compounds useful for the treatment of degenerative and inflammatory diseases
WO2010010188A1 (en) 2008-07-25 2010-01-28 Galapagos Nv Novel compounds useful for the treatment of degenerative and inflammatory diseases.
WO2010010189A1 (en) 2008-07-25 2010-01-28 Galapagos Nv Novel compounds useful for the treatment of degenerative and inflammatory diseases
WO2010010184A1 (en) 2008-07-25 2010-01-28 Galapagos Nv [1, 2, 4] triazolo [1, 5-a] pyridines as jak inhibitors
UY32049A (es) 2008-08-14 2010-03-26 Takeda Pharmaceutical Inhibidores de cmet
TR200806298A2 (tr) 2008-08-22 2010-03-22 Bi̇lgi̇ç Mahmut Farmasötik formülasyon
US20120021519A1 (en) 2008-09-19 2012-01-26 Presidents And Fellows Of Harvard College Efficient induction of pluripotent stem cells using small molecule compounds
JP2010070503A (ja) 2008-09-19 2010-04-02 Daiichi Sankyo Co Ltd 抗真菌作用２−アミノトリアゾロピリジン誘導体
WO2010036380A1 (en) 2008-09-26 2010-04-01 Intellikine, Inc. Heterocyclic kinase inhibitors
WO2010043721A1 (en) 2008-10-17 2010-04-22 Oryzon Genomics, S.A. Oxidase inhibitors and their use
WO2010048149A2 (en) 2008-10-20 2010-04-29 Kalypsys, Inc. Heterocyclic modulators of gpr119 for treatment of disease
DK2376490T3 (da) 2008-12-04 2013-04-15 Proximagen Ltd Imidazopyridinforbindelser
US8450321B2 (en) 2008-12-08 2013-05-28 Gilead Connecticut, Inc. 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
EP2389362B1 (de) 2009-01-21 2019-12-11 Oryzon Genomics, S.A. Phenylcyclopropylaminderivate und deren medizinische verwendung
EP2393813B1 (de) 2009-02-04 2013-07-31 Vitae Pharmaceuticals, Inc. Zur Behandlung von durch erhöhten Cortisonspiegel bedingten Krankheiten geeignete cyclische Inhibitoren von 11 ß-Hydroxysteroiddehydrogenase 1
US20100209489A1 (en) 2009-02-04 2010-08-19 Supernus Pharmaceuticals, Inc. Formulations of desvenlafaxine
TR200900879A2 (tr) 2009-02-05 2010-08-23 Bi̇lgi̇ç Mahmut Aktif maddelerin tek bir dozaj formunda kombine edildiği farmasötik bileşimler
TR200900878A2 (tr) 2009-02-05 2010-08-23 Bi̇lgi̇ç Mahmut Tek bir dozaj formunda kombine edilen farmasötik formülasyonlar
US20130310362A1 (en) 2009-02-13 2013-11-21 Bayer Pharma Aktiegesellschaft Fused pyrimidines
KR20100101055A (ko) 2009-03-07 2010-09-16 주식회사 메디젠텍 세포핵에서 세포질로의 ｇｓｋ３의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 ｇｓｋ３ 이동 관련 질환의 치료 또는 예방용 약학적 조성물
WO2010107404A1 (en) 2009-03-16 2010-09-23 Mahmut Bilgic Stable pharmaceutical combinations
US8481732B2 (en) 2009-03-20 2013-07-09 Incyte Corporation Substituted heterocyclic compounds
ES2429148T3 (es) 2009-03-31 2013-11-13 Kissei Pharmaceutical Co., Ltd. Derivado de indolizina y su utilización para fines médicos
ES2475091T3 (es) 2009-04-16 2014-07-10 Centro Nacional De Investigaciones Oncol�Gicas (Cnio) Imidazopirazinas como inhibidores de proteína cinasas
TWI461426B (zh) 2009-05-27 2014-11-21 Merck Sharp & Dohme （二氫）咪唑並異〔５，１－ａ〕喹啉類
JP2012529529A (ja) 2009-06-10 2012-11-22 スノビオン プハルマセウトイカルス インコーポレイテッド ヒスタミンｈ３インバースアゴニスト及びアンタゴニスト、並びにその使用方法
WO2010151711A1 (en) 2009-06-25 2010-12-29 Alkermes, Inc. Prodrugs of nh-acidic compounds
ES2709108T3 (es) 2009-08-17 2019-04-15 Intellikine Llc Compuestos heterocíclicos y usos de los mismos
EP2467359A4 (de) 2009-08-18 2013-01-09 Univ Johns Hopkins (bis-)harnstoff- und (bis-)thioharnstoffverbindungen als epigene modulatoren der lysinspezifischen demethylase 1 sowie verfahren zur krankheitsbehandlung damit
US8546376B2 (en) 2009-09-18 2013-10-01 Almac Discovery Limited Pharmaceutical compounds
CN102639496B (zh) 2009-09-25 2014-10-29 奥瑞泽恩基因组学股份有限公司 赖氨酸特异性脱甲基酶-1抑制剂及其应用
EP2486002B1 (de) 2009-10-09 2019-03-27 Oryzon Genomics, S.A. Substituierte heteroaryl- und arylcyclopropylaminacetamide und ihre verwendung
WO2011050245A1 (en) 2009-10-23 2011-04-28 Yangbo Feng Bicyclic heteroaryls as kinase inhibitors
US8541404B2 (en) 2009-11-09 2013-09-24 Elexopharm Gmbh Inhibitors of the human aldosterone synthase CYP11B2
US8614315B2 (en) 2009-12-25 2013-12-24 Mahmut Bilgic Cefdinir and cefixime formulations and uses thereof
EP2526102B1 (de) 2010-01-22 2017-03-08 Fundación Centro Nacional de Investigaciones Oncológicas Carlos III PI3-kinase-inhibitoren
WO2011097607A1 (en) 2010-02-08 2011-08-11 Southern Research Institute Anti-viral treatment and assay to screen for anti-viral agent
WO2011106573A2 (en) 2010-02-24 2011-09-01 Oryzon Genomics, S.A. Lysine demethylase inhibitors for diseases and disorders associated with hepadnaviridae
US9616058B2 (en) 2010-02-24 2017-04-11 Oryzon Genomics, S.A. Potent selective LSD1 inhibitors and dual LSD1/MAO-B inhibitors for antiviral use
TW201200518A (en) 2010-03-10 2012-01-01 Kalypsys Inc Heterocyclic inhibitors of histamine receptors for the treatment of disease
PL2547678T3 (pl) 2010-03-18 2016-10-31 Związki przeciwzapalne
EP2547680B1 (de) 2010-03-18 2015-08-05 Bayer Intellectual Property GmbH Imidazopyrazine
SI2552920T1 (sl) 2010-04-02 2017-07-31 Ogeda Sa Nove nk-3 receptor selektivne antagonist spojine, farmacevtski sestavki in postopki za uporabo pri nk-3 receptor posredovanih motnjah
BR112012026694A2 (pt) 2010-04-19 2016-07-12 Oryzon Genomics Sa inibidores da desmetilase específica para lisina 1 e seu uso
JP5934184B2 (ja) 2010-04-20 2016-06-15 ウニヴェルシタ・デグリ・ストゥディ・ディ・ローマ・ラ・サピエンツァ ヒストンデメチラーゼｌｓｄ１及び／又はｌｓｄ２の阻害剤としてのトラニルシプロミン誘導体
JPWO2011136264A1 (ja) 2010-04-28 2013-07-22 第一三共株式会社 ［５，６］複素環化合物
EA201291236A1 (ru) 2010-05-13 2013-11-29 Эмджен Инк. Азотные гетероциклические соединения, применимые в качестве ингибиторов pde10
US20130131057A1 (en) 2010-05-13 2013-05-23 Centro Nacional De Investigaciones Oncologicas (Cnio New bicyclic compounds as pi3-k and mtor inhibitors
CN102247321A (zh) 2010-05-20 2011-11-23 上海亚盛医药科技有限公司 一种阿朴棉子酚酮自乳化药物传递系统及其制备方法
EP2575808A1 (de) 2010-05-28 2013-04-10 Mahmut Bilgic Kombination aus blutdrucksenkenden mitteln
CN102295642B (zh) 2010-06-25 2016-04-06 中国人民解放军军事医学科学院毒物药物研究所 2-芳基咪唑并[1,2-a]吡啶-3-乙酰胺衍生物、其制备方法及用途
CN103096977B (zh) 2010-07-02 2017-02-15 吉利德科学公司 作为离子通道调节剂的稠杂环化合物
EP2593451B1 (de) 2010-07-12 2015-08-19 Bayer Intellectual Property GmbH Substituierte imidazo[1,2-a]pyrimidine und -pyridine
WO2012009475A1 (en) 2010-07-14 2012-01-19 Oregon Health & Science University Methods of treating cancer with inhibition of lysine-specific demethylase 1
CN101987082B (zh) 2010-07-16 2013-04-03 钟术光 固体制剂及其制备方法
CN101987081B (zh) 2010-07-16 2012-08-08 钟术光 一种控释制剂
WO2012013728A1 (en) 2010-07-29 2012-02-02 Oryzon Genomics S.A. Arylcyclopropylamine based demethylase inhibitors of lsd1 and their medical use
WO2012013727A1 (en) 2010-07-29 2012-02-02 Oryzon Genomics S.A. Cyclopropylamine derivatives useful as lsd1 inhibitors
WO2012016133A2 (en) 2010-07-29 2012-02-02 President And Fellows Of Harvard College Ros1 kinase inhibitors for the treatment of glioblastoma and other p53-deficient cancers
CN102397552B (zh) 2010-09-10 2016-06-08 广州自远生物科技有限公司 一种含喹诺酮类的药物复合制剂及其制备方法和应用
US9527805B2 (en) 2010-09-10 2016-12-27 Robert A. Casero Small molecules as epigenetic modulators of lysine-specific demethylase 1 and methods of treating disorders
CA2811773A1 (en) 2010-09-29 2012-04-05 Kissei Pharmaceutical Co., Ltd. (aza)indolizine derivative and pharmaceutical use thereof
US20130303545A1 (en) 2010-09-30 2013-11-14 Tamara Maes Cyclopropylamine derivatives useful as lsd1 inhibitors
JP2013540767A (ja) 2010-10-07 2013-11-07 ザ ジェイ． デヴィッド グラッドストーン インスティテューツ 免疫不全ウイルス転写を調節するための組成物および方法
WO2012054233A1 (en) 2010-10-18 2012-04-26 E. I. Du Pont De Nemours And Company Nematocidal sulfonamides
WO2012052745A1 (en) 2010-10-21 2012-04-26 Centro Nacional De Investigaciones Oncológicas (Cnio) Combinations of pi3k inhibitors with a second anti -tumor agent
AR083502A1 (es) 2010-10-21 2013-02-27 Biomarin Pharm Inc Sal tosilada de (8s,9r)-5-fluoro-8-(4-fluorofenil)-9-(1-metil-1h-1,2,4-triazol-5-il)-8,9-dihidro-2h-pirido[4,3,2-de]ftalazin-3(7h)-ona cristalina
EP2444084A1 (de) 2010-10-21 2012-04-25 Centro Nacional de Investigaciones Oncológicas (CNIO) Verwendung von PI3K Inhibitoren zur Behandlung der Fettleibigkeit
WO2012071469A2 (en) 2010-11-23 2012-05-31 Nevada Cancer Institute Histone demethylase inhibitors and uses thereof for treatment o f cancer
WO2012072713A2 (en) 2010-11-30 2012-06-07 Oryzon Genomics, S.A. Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae
JP2014503528A (ja) 2010-12-14 2014-02-13 エレクトロプホレトイクス リミテッド カゼインキナーゼ１δ（ＣＫ１δ）阻害剤及びタウオパチーなどの神経変性疾患の治療におけるその使用
CN103443100B (zh) 2010-12-17 2016-03-23 拜耳知识产权有限责任公司 在过度增殖性病症的治疗中用作mps-1和tkk抑制剂的取代的6-咪唑并吡嗪
CA2821819A1 (en) 2010-12-17 2012-06-21 Marcus Koppitz 6-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
UY33805A (es) 2010-12-17 2012-07-31 Boehringer Ingelheim Int ?Derivados de dihidrobenzofuranil-piperidinilo, aza-dihidrobenzofuranilpiperidinilo y diaza-dihidrobenzofuranil-piperidinilo, composiciones farmacéuticas que los contienen y usos de los mismos?.
CN103370322B (zh) 2010-12-17 2016-02-10 拜耳知识产权有限责任公司 在过度增殖性病症的治疗中用作mps-1和tkk抑制剂的2-取代的咪唑并吡嗪
US20140187548A1 (en) 2010-12-17 2014-07-03 Bayer Intellectual Property Gmbh 6 substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
US8987271B2 (en) 2010-12-22 2015-03-24 Eutropics Pharmaceuticals, Inc. 2,2′-biphenazine compounds and methods useful for treating disease
TWI617559B (zh) 2010-12-22 2018-03-11 江蘇恆瑞醫藥股份有限公司 ２－芳基咪唑并［１，２－ｂ］嗒．２－苯基咪唑并［１，２－ａ］吡啶，和２－苯基咪唑并［１，２－ａ］吡衍生物
EP2665726A4 (de) 2011-01-21 2014-09-03 Gen Hospital Corp Zusammensetzungen und verfahren zur behandlung kardiovaskulärer erkrankungen
WO2012107498A1 (en) 2011-02-08 2012-08-16 Oryzon Genomics S.A. Lysine demethylase inhibitors for myeloproliferative disorders
WO2012107499A1 (en) 2011-02-08 2012-08-16 Oryzon Genomics S.A. Lysine demethylase inhibitors for myeloproliferative or lymphoproliferative diseases or disorders
US9127000B2 (en) 2011-02-23 2015-09-08 Intellikine, LLC. Heterocyclic compounds and uses thereof
US9464065B2 (en) 2011-03-24 2016-10-11 The Scripps Research Institute Compounds and methods for inducing chondrogenesis
KR101884493B1 (ko) 2011-03-25 2018-08-01 글락소스미스클라인 인털렉츄얼 프로퍼티 (넘버 2) 리미티드 Lsd1 억제제로서의 시클로프로필아민
WO2012147890A1 (ja) 2011-04-27 2012-11-01 持田製薬株式会社 新規アゾール誘導体
EP2524918A1 (de) 2011-05-19 2012-11-21 Centro Nacional de Investigaciones Oncológicas (CNIO) Imidazopyrazinderivate als Kinase Inhibitoren
US20140329833A1 (en) 2011-05-19 2014-11-06 Oryzon Genomics, S.A Lysine demethylase inhibitors for inflammatory diseases or conditions
EP2750671A2 (de) 2011-05-19 2014-07-09 Oryzon Genomics, S.A. Lysin-demethylaseinhibitoren für thrombosen und herz-kreislauf-erkrankungen
CN103687496A (zh) 2011-06-07 2014-03-26 Spai集团有限公司 用于改善敏感性食品添加剂及其食品产品的稳定性并且延长其货架期的组合物和方法
EP2721028B1 (de) 2011-06-20 2015-11-04 Incyte Corporation Azetidinylphenyl-, pyridyl- oder pyrazinylcarboxamidderivate als jak-inhibitoren
TW201311149A (zh) 2011-06-24 2013-03-16 Ishihara Sangyo Kaisha 有害生物防治劑
EP2548877A1 (de) 2011-07-19 2013-01-23 MSD Oss B.V. 4-(5-Gliedrige kondensierte Pyridinyl)benzamide als BTK-Inhibitoren
CN103842332B (zh) 2011-08-09 2016-08-17 武田药品工业株式会社 环丙胺化合物
EP2744330B1 (de) 2011-08-15 2020-07-15 University of Utah Research Foundation Substituierte (e) -n'- (1-phenylethylidene) benzohydrazid-analoga als histondemethylase-hemmer
WO2013033688A1 (en) 2011-09-01 2013-03-07 The Brigham And Women's Hospital, Inc. Treatment of cancer
US9273343B2 (en) 2011-09-02 2016-03-01 Promega Corporation Compounds and methods for assaying redox state of metabolically active cells and methods for measuring NAD(P)/NAD(P)H
JP2015531401A (ja) 2011-10-10 2015-11-02 ハー・ルンドベック・アクチエゼルスカベット イミダゾピラジノン骨格を有するｐｄｅ９ｉ
CL2014000988A1 (es) 2011-10-20 2014-11-03 Oryzon Genomics Sa Compuestos derivados de (aril o heteroaril) ciclopropilamida, inhibidores de lsd1; procedimiento para prepararlos; composicion farmaceutica que los comprende; y metodo para tratar o prevenir cancer, una enfermedad neurologica, una infeccion viral y la reactivacion viral despues de la latencia.
SG11201401066PA (en) 2011-10-20 2014-10-30 Oryzon Genomics Sa (hetero)aryl cyclopropylamine compounds as lsd1 inhibitors
RU2681211C2 (ru) * 2011-10-20 2019-03-05 Оризон Дженомикс С.А. (гетеро)арилциклопропиламины в качестве ингибиторов lsd1
ITMI20111971A1 (it) 2011-10-28 2013-04-29 Mesogenics Srl Inibitori dell'enzima lsd-1 per l'induzione del differenziamento osteogenico
EP2785183B1 (de) 2011-11-14 2018-12-19 Merck Sharp & Dohme Corp. Triazolpyridinon-pde10-inhibitoren
US20140288145A1 (en) 2011-12-05 2014-09-25 Brandeis University Treatment of amyloidosis by compounds that regulate retromer stabilization
EP2822948B1 (de) 2012-03-07 2016-04-06 Merck Patent GmbH Triazolopyrazinderivate
CN102587054B (zh) 2012-03-13 2014-05-07 机械科学研究总院先进制造技术研究中心 缸盖自动锁紧装置及包括该装置的筒子纱染色机
GB201205669D0 (en) 2012-03-30 2012-05-16 Agency Science Tech & Res Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof
CN102579381B (zh) 2012-03-30 2013-07-10 河南中帅医药科技发展有限公司 盐酸胍法辛缓释制剂及其制备方法
CN103373996A (zh) 2012-04-20 2013-10-30 山东亨利医药科技有限责任公司 作为crth2受体拮抗剂的二并环衍生物
WO2014002051A2 (en) 2012-06-28 2014-01-03 Novartis Ag Complement pathway modulators and uses thereof
CN102772444A (zh) 2012-07-06 2012-11-14 周明千 中药超微破壁口服片剂饮片的加工方法
GB201212513D0 (en) 2012-07-13 2012-08-29 Ucb Pharma Sa Therapeutic agents
JP6430383B2 (ja) 2012-09-28 2018-11-28 ヴァンダービルト ユニバーシティーＶａｎｄｅｒｂｉｌｔ Ｕｎｉｖｅｒｓｉｔｙ 選択的ｂｍｐ阻害剤としての縮合複素環化合物
CN104837832B (zh) 2012-10-05 2019-04-26 里格尔药品股份有限公司 Gdf-8抑制剂
US9751885B2 (en) * 2012-10-12 2017-09-05 Takeda Pharmaceutical Company Limited Cyclopropanamine compound and use thereof
EP2919770A4 (de) 2012-11-14 2017-03-08 The Board of Regents of The University of Texas System Hemmung einer hif-2 heterodimerisierung mit hif1 (arnt)
JP6238908B2 (ja) 2012-11-28 2017-11-29 京都府公立大学法人 リシン構造を有するｌｓｄ１選択的阻害薬
CA2892375A1 (en) 2012-11-30 2014-06-05 Darlene E. MCCORD Hydroxytyrosol and oleuropein compositions for induction of dna damage, cell death and lsd1 inhibition
EP2740474A1 (de) 2012-12-05 2014-06-11 Instituto Europeo di Oncologia S.r.l. Cyclopropylaminderivate als Hemmer von Histon-Demethylase-KDM1A
US9707275B2 (en) 2012-12-19 2017-07-18 Wockhardt Limited Stable aqueous composition comprising human insulin or an analogue or derivative thereof
CN103054869A (zh) 2013-01-18 2013-04-24 郑州大学 含三唑基的氨基二硫代甲酸酯化合物在制备以lsd1为靶标药物中的应用
CN103933036B (zh) 2013-01-23 2017-10-13 中国人民解放军军事医学科学院毒物药物研究所 2‑芳基咪唑并[1,2‑α]吡啶‑3‑乙酰胺衍生物在制备防治PTSD的药物中的用途
EP2956441A4 (de) 2013-02-18 2016-11-02 Scripps Research Inst Modulatoren der vasopressin-rezeptoren mit therapeutischem potenzial
US8558008B2 (en) 2013-02-28 2013-10-15 Dermira, Inc. Crystalline glycopyrrolate tosylate
WO2014164867A1 (en) 2013-03-11 2014-10-09 Imago Biosciences Kdm1a inhibitors for the treatment of disease
AU2014231768A1 (en) 2013-03-13 2015-09-24 Australian Nuclear Science And Technology Organisation Transgenic non-human organisms with non-functional TSPO genes
US20140343118A1 (en) 2013-03-14 2014-11-20 Duke University Methods of treatment using arylcyclopropylamine compounds
CA2903312A1 (en) 2013-03-14 2014-09-25 Epizyme, Inc. Combination therapy for treating cancer
EP3003301B1 (de) 2013-05-30 2021-02-24 Board Of Regents Of The Nevada System Of Higher Education On Behalf Of The University Of Nevada, Las Vegas Neuartige, gegen sox2-exprimierende krebszellen gerichtete lsd1-suizidinhibitoren
BR112015032113B1 (pt) 2013-06-19 2019-01-29 University Of Utah Research Foundation análogos de (e)-n’-(1-feniletilideno)benzohidrazida substituídos como inibidores de histona demetilase
MY190860A (en) 2013-06-21 2022-05-12 Myokardia Inc Pyrimidinedione compounds against cardiac conditions
US9186391B2 (en) 2013-08-29 2015-11-17 Musc Foundation For Research Development Cyclic peptide inhibitors of lysine-specific demethylase 1
WO2015031564A2 (en) 2013-08-30 2015-03-05 University Of Utah Substituted-1h-benzo[d]imidazole series compounds as lysine-specfic demethylase 1 (lsd1) inhibitors
US9770514B2 (en) 2013-09-03 2017-09-26 ExxPharma Therapeutics LLC Tamper-resistant pharmaceutical dosage forms
DK3043778T3 (da) 2013-09-13 2017-11-27 Bayer Pharma AG Farmaceutiske sammensætninger, der indeholder refametinib
KR101568724B1 (ko) 2013-11-13 2015-11-12 서울대학교산학협력단 신규한 화합물, 이의 생산 방법, 및 히스톤 디메틸라제 저해제로서 이의 용도
HRP20230086T1 (hr) 2013-12-11 2023-03-31 Celgene Quanticel Research, Inc. Inhibitori lizin specifične demetilaze-1
TWI664164B (zh) 2014-02-13 2019-07-01 美商英塞特控股公司 作為ｌｓｄ１抑制劑之環丙胺
US9346776B2 (en) 2014-02-13 2016-05-24 Takeda Pharmaceutical Company Limited Fused heterocyclic compound
JP6602778B2 (ja) 2014-02-13 2019-11-06 インサイト・コーポレイション Ｌｓｄ１阻害剤としてのシクロプロピルアミン類
US9527835B2 (en) 2014-02-13 2016-12-27 Incyte Corporation Cyclopropylamines as LSD1 inhibitors
WO2015123408A1 (en) 2014-02-13 2015-08-20 Incyte Corporation Cyclopropylamines as lsd1 inhibitors
US9428470B2 (en) 2014-02-13 2016-08-30 Takeda Pharmaceutical Company Limited Heterocyclic compound
CN103893163B (zh) 2014-03-28 2016-02-03 中国药科大学 2-([1，1′-联苯]-4-基)2-氧代乙基4-((3-氯-4-甲基苯基)氨基)-4-氧代丁酸酯在制备lsd1抑制剂药物中的应用
PL3126351T3 (pl) 2014-04-02 2019-03-29 Bristol-Myers Squibb Company Biarylowe inhibitory kinazy
EP2933002A1 (de) 2014-04-11 2015-10-21 Sanovel Ilac Sanayi ve Ticaret A.S. Pharmazeutische kombinationen von dabigatran und protonenpumpeninhibitoren
CR20160485A (es) 2014-04-11 2017-01-02 Takeda Pharmaceuticals Co Compuesto de ciclopropanamina y sus usos
WO2015155297A1 (en) 2014-04-11 2015-10-15 Sanovel Ilac Sanayi Ve Ticaret A.S. Pharmaceutical combinations of dabigatran and h2-receptor antagonists
CN103961340B (zh) 2014-04-30 2019-06-25 南通中国科学院海洋研究所海洋科学与技术研究发展中心 一类lsd1抑制剂及其应用
US10233165B2 (en) 2014-05-30 2019-03-19 Istituto Europeo Di Oncologia S.R.L. Cyclopropylamine compounds as histone demethylase inhibitors
CN104119280B (zh) 2014-06-27 2016-03-16 郑州大学 含氨基类脲与端炔结构单元的嘧啶衍生物、制备方法及应用
WO2016007727A1 (en) 2014-07-10 2016-01-14 Incyte Corporation Triazolopyridines and triazolopyrazines as lsd1 inhibitors
TWI687419B (zh) 2014-07-10 2020-03-11 美商英塞特公司 作為ｌｓｄ１抑制劑之咪唑并吡啶及咪唑并吡嗪
US9695167B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors
TW201613925A (en) 2014-07-10 2016-04-16 Incyte Corp Imidazopyrazines as LSD1 inhibitors
GB201417828D0 (en) 2014-10-08 2014-11-19 Cereno Scient Ab New methods and compositions
CN104173313B (zh) 2014-08-25 2017-05-17 杭州朱养心药业有限公司 利伐沙班片剂药物组合物
JP6653116B2 (ja) 2014-08-27 2020-02-26 日本ケミファ株式会社 オルメサルタンのプロドラッグ製剤
EP3204383B1 (de) 2014-10-08 2020-11-18 F.Hoffmann-La Roche Ag Spirodiamin-derivate als aldosteron-synthase-hemmer
SG11201708047UA (en) 2015-04-03 2017-10-30 Incyte Corp Heterocyclic compounds as lsd1 inhibitors
JP2018510198A (ja) 2015-04-03 2018-04-12 ミュタビリスＭｕｔａｂｉｌｉｓ 複素環式化合物及びそれらの細菌感染症の予防または治療のための使用
US10399933B2 (en) 2015-04-03 2019-09-03 Bristol-Myers Squibb Company Inhibitors of indoleamine-2,3-dioxygenase for the treatment of cancer
EP3334709A1 (de) 2015-08-12 2018-06-20 Incyte Corporation Salze eines lsd1-hemmers
CN112656772B (zh) 2015-10-15 2022-05-20 浙江东日药业有限公司 利伐沙班药物组合物
AU2016382463B2 (en) 2015-12-29 2021-05-27 Mirati Therapeutics, Inc. LSD1 inhibitors
WO2017130933A1 (ja) 2016-01-25 2017-08-03 国立大学法人熊本大学 神経変性疾患治療剤
WO2017184934A1 (en) 2016-04-22 2017-10-26 Incyte Corporation Formulations of an lsd1 inhibitor
CN110430880A (zh) 2017-01-18 2019-11-08 范德比尔特大学 作为选择性bmp抑制剂的稠合杂环化合物
JP7111733B2 (ja) 2017-03-16 2022-08-02 江蘇恒瑞医薬股▲ふん▼有限公司 ヘテロアリール［４，３－ｃ］ピリミジン－５－アミン誘導体、その製造方法、およびその医薬の使用
WO2020010197A1 (en) 2018-07-05 2020-01-09 Incyte Corporation Fused pyrazine derivatives as a2a / a2b inhibitors
US10968200B2 (en) 2018-08-31 2021-04-06 Incyte Corporation Salts of an LSD1 inhibitor and processes for preparing the same

Also Published As

Publication number Publication date
JP6781815B2 (ja) 2020-11-04
KR20160138000A (ko) 2016-12-02
SI3105226T1 (sl) 2019-11-29
PE20161384A1 (es) 2016-12-28
BR112016018555A8 (pt) 2023-01-24
MX2016010390A (es) 2017-02-27
IL277299A (en) 2020-10-29
MX2020003702A (es) 2020-07-22
BR112016018555B1 (pt) 2024-01-23
JP2021011496A (ja) 2021-02-04
AU2015217119C1 (en) 2020-01-16
US11155532B2 (en) 2021-10-26
US9493450B2 (en) 2016-11-15
CL2016002021A1 (es) 2016-12-23
HUE045725T2 (hu) 2020-01-28
HRP20192033T1 (hr) 2020-02-07
CN106488915B (zh) 2020-10-02
CR20160395A (es) 2016-12-20
PL3105226T3 (pl) 2020-03-31
ES2750956T3 (es) 2020-03-30
UA122389C2 (uk) 2020-11-10
CN106488915A (zh) 2017-03-08
IL246950B (en) 2020-09-30
TW201620875A (zh) 2016-06-16
SG11201606333VA (en) 2016-09-29
KR102352408B1 (ko) 2022-01-18
TWI720451B (zh) 2021-03-01
US9994546B2 (en) 2018-06-12
US20170121302A1 (en) 2017-05-04
DK3105226T3 (da) 2019-10-14
JP2017510555A (ja) 2017-04-13
IL277299B (en) 2022-04-01
JP6602779B2 (ja) 2019-11-06
WO2015123424A1 (en) 2015-08-20
IL246950A0 (en) 2016-09-29
AU2019204244B2 (en) 2021-04-08
NZ723203A (en) 2020-08-28
CA2939081C (en) 2023-08-15
US10676457B2 (en) 2020-06-09
US20210024487A1 (en) 2021-01-28
BR112016018555A2 (de) 2017-08-08
CR20200362A (es) 2020-10-26
MY196877A (en) 2023-05-08
RS59534B1 (sr) 2019-12-31
EA201691594A1 (ru) 2017-02-28
AU2015217119B2 (en) 2019-07-11
ECSP16073171A (es) 2017-03-31
SG10201806846RA (en) 2018-09-27
CA2939081A1 (en) 2015-08-20
ME03580B (de) 2020-07-20
PT3105226T (pt) 2019-11-06
US20150225394A1 (en) 2015-08-13
AU2015217119A1 (en) 2016-09-01
AU2019204244A1 (en) 2019-07-04
CY1122314T1 (el) 2021-01-27
TW201940466A (zh) 2019-10-16
JP2020023529A (ja) 2020-02-13
LT3105226T (lt) 2019-11-11
TWI664164B (zh) 2019-07-01
US20190062301A1 (en) 2019-02-28
PH12016501546B1 (en) 2016-10-03
EP3105226B1 (de) 2019-09-04
EP3626714A1 (de) 2020-03-25
PH12016501546A1 (en) 2016-10-03

Similar Documents

Publication Publication Date Title
US11155532B2 (en) Cyclopropylamines as LSD1 inhibitors
US11247992B2 (en) Cyclopropylamines as LSD1 inhibitors
US10513493B2 (en) Cyclopropylamines as LSD1 inhibitors
US9493442B2 (en) Cyclopropylamines as LSD1 inhibitors
JP2020023529A6 (ja) Ｌｓｄ１阻害剤としてのシクロプロピルアミン類

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20160908

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

RIN1 Information on inventor provided before grant (corrected)

Inventor name: KONKOL, LEAH C.

Inventor name: HE, CHUNHONG

Inventor name: SHEN, BO

Inventor name: QIAN, DING-QUAN

Inventor name: WU, LIANGXING

Inventor name: ZHANG, FENGLEI

Inventor name: YAO, WENQING

Inventor name: COURTER, JOEL R.

REG Reference to a national code

Ref country code: HK

Ref legal event code: DE

Ref document number: 1231063

Country of ref document: HK

17Q First examination report despatched

Effective date: 20180227

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20181109

GRAJ Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted

Free format text: ORIGINAL CODE: EPIDOSDIGR1

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTC Intention to grant announced (deleted)
INTG Intention to grant announced

Effective date: 20190403

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1175146

Country of ref document: AT

Kind code of ref document: T

Effective date: 20190915

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602015037109

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

Effective date: 20191010

REG Reference to a national code

Ref country code: CH

Ref legal event code: NV

Representative=s name: E. BLUM AND CO. AG PATENT- UND MARKENANWAELTE , CH

REG Reference to a national code

Ref country code: PT

Ref legal event code: SC4A

Ref document number: 3105226

Country of ref document: PT

Date of ref document: 20191106

Kind code of ref document: T

Free format text: AVAILABILITY OF NATIONAL TRANSLATION

Effective date: 20191030

REG Reference to a national code

Ref country code: HR

Ref legal event code: TUEP

Ref document number: P20192033T

Country of ref document: HR

REG Reference to a national code

Ref country code: RO

Ref legal event code: EPE

REG Reference to a national code

Ref country code: NL

Ref legal event code: FP

REG Reference to a national code

Ref country code: NO

Ref legal event code: T2

Effective date: 20190904

REG Reference to a national code

Ref country code: SE

Ref legal event code: TRGR

REG Reference to a national code

Ref country code: HU

Ref legal event code: AG4A

Ref document number: E045725

Country of ref document: HU

REG Reference to a national code

Ref country code: SK

Ref legal event code: T3

Ref document number: E 32813

Country of ref document: SK

REG Reference to a national code

Ref country code: HR

Ref legal event code: T1PR

Ref document number: P20192033

Country of ref document: HR

REG Reference to a national code

Ref country code: EE

Ref legal event code: FG4A

Ref document number: E018464

Country of ref document: EE

Effective date: 20191128

REG Reference to a national code

Ref country code: HR

Ref legal event code: ODRP

Ref document number: P20192033

Country of ref document: HR

Payment date: 20200122

Year of fee payment: 6

REG Reference to a national code

Ref country code: GR

Ref legal event code: EP

Ref document number: 20190403601

Country of ref document: GR

Effective date: 20200213

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2750956

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20200330

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602015037109

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20200605

REG Reference to a national code

Ref country code: AT

Ref legal event code: UEP

Ref document number: 1175146

Country of ref document: AT

Kind code of ref document: T

Effective date: 20190904

REG Reference to a national code

Ref country code: HR

Ref legal event code: ODRP

Ref document number: P20192033

Country of ref document: HR

Payment date: 20210120

Year of fee payment: 7

REG Reference to a national code

Ref country code: HR

Ref legal event code: ODRP

Ref document number: P20192033

Country of ref document: HR

Payment date: 20220118

Year of fee payment: 8

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

Free format text: REGISTERED BETWEEN 20220616 AND 20220622

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602015037109

Country of ref document: DE

Owner name: INCYTE HOLDINGS CORPORATION, WILMINGTON, US

Free format text: FORMER OWNER: INCYTE CORP., WILMINGTON, DEL., US

REG Reference to a national code

Ref country code: LU

Ref legal event code: PD

Owner name: INCYTE HOLDINGS CORPORATION; US

Free format text: FORMER OWNER: INCYTE CORPORATION

Effective date: 20221018

REG Reference to a national code

Ref country code: BE

Ref legal event code: PD

Owner name: INCYTE HOLDINGS CORPORATION; US

Free format text: DETAILS ASSIGNMENT: CHANGE OF OWNER(S), ASSIGNMENT; FORMER OWNER NAME: INCYTE CORPORATION

Effective date: 20221109

REG Reference to a national code

Ref country code: HR

Ref legal event code: ODRP

Ref document number: P20192033

Country of ref document: HR

Payment date: 20230119

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CY

Payment date: 20230120

Year of fee payment: 9

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230525

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AL

Payment date: 20230220

Year of fee payment: 9

REG Reference to a national code

Ref country code: HR

Ref legal event code: ODRP

Ref document number: P20192033

Country of ref document: HR

Payment date: 20240129

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20240129

Year of fee payment: 10

Ref country code: MK

Payment date: 20230118

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: LU

Payment date: 20240129

Year of fee payment: 10

REG Reference to a national code

Ref country code: HU

Ref legal event code: GB9C

Owner name: INCYTE HOLDINGS CORPORATION, US

Free format text: FORMER OWNER(S): INCYTE CORPORATION, US

Ref country code: HU

Ref legal event code: FH1C

Free format text: FORMER REPRESENTATIVE(S): DANUBIA SZABADALMI ES JOGI IRODA KFT., HU

Representative=s name: DANUBIA SZABADALMI ES JOGI IRODA KFT., HU

REG Reference to a national code

Ref country code: NL

Ref legal event code: PD

Owner name: INCYTE HOLDINGS CORPORATION; US

Free format text: DETAILS ASSIGNMENT: CHANGE OF OWNER(S), ASSIGNMENT; FORMER OWNER NAME: INCYTE CORPORATION

Effective date: 20240326

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GR

Payment date: 20240130

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IS

Payment date: 20240131

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: LT

Payment date: 20240119

Year of fee payment: 10

REG Reference to a national code

Ref country code: EE

Ref legal event code: GB1A

Ref document number: E018464

Country of ref document: EE

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20240307

Year of fee payment: 10

Ref country code: IE

Payment date: 20240124

Year of fee payment: 10

REG Reference to a national code

Ref country code: HR

Ref legal event code: PPPP

Ref document number: P20192033

Country of ref document: HR

Owner name: INCYTE HOLDINGS CORPORATION, US

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AT

Payment date: 20240125

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: MC

Payment date: 20240126

Year of fee payment: 10

REG Reference to a national code

Ref country code: SK

Ref legal event code: PC4A

Ref document number: E 32813

Country of ref document: SK

Owner name: INCYTE HOLDINGS CORPORATION, WILMINGTON, DE, US

Free format text: FORMER OWNER: INCYTE CORPORATION, WILMINGTON, DE, US

Effective date: 20240405

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SM

Payment date: 20240229

Year of fee payment: 10

Ref country code: RO

Payment date: 20240131

Year of fee payment: 10

Ref country code: HU

Payment date: 20240205

Year of fee payment: 10

Ref country code: FI

Payment date: 20240213

Year of fee payment: 10

Ref country code: EE

Payment date: 20240122

Year of fee payment: 10

Ref country code: DE

Payment date: 20240124

Year of fee payment: 10

Ref country code: CZ

Payment date: 20240126

Year of fee payment: 10

Ref country code: BG

Payment date: 20240130

Year of fee payment: 10

Ref country code: GB

Payment date: 20240118

Year of fee payment: 10

Ref country code: PT

Payment date: 20240211

Year of fee payment: 10

Ref country code: CH

Payment date: 20240301

Year of fee payment: 10

Ref country code: SK

Payment date: 20240123

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SI

Payment date: 20240124

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: TR

Payment date: 20240129

Year of fee payment: 10

Ref country code: SE

Payment date: 20240130

Year of fee payment: 10

Ref country code: RS

Payment date: 20240202

Year of fee payment: 10

Ref country code: PL

Payment date: 20240119

Year of fee payment: 10

Ref country code: NO

Payment date: 20240208

Year of fee payment: 10

Ref country code: MT

Payment date: 20240214

Year of fee payment: 10

Ref country code: LV

Payment date: 20240119

Year of fee payment: 10

Ref country code: IT

Payment date: 20240126

Year of fee payment: 10

Ref country code: HR

Payment date: 20240129

Year of fee payment: 10

Ref country code: FR

Payment date: 20240123

Year of fee payment: 10

Ref country code: DK

Payment date: 20240214

Year of fee payment: 10

Ref country code: BE

Payment date: 20240129

Year of fee payment: 10

REG Reference to a national code

Ref country code: SI

Ref legal event code: SP73

Owner name: INCYTE HOLDINGS CORPORATION; US

Effective date: 20240423

REG Reference to a national code

Ref country code: AT

Ref legal event code: PC

Ref document number: 1175146

Country of ref document: AT

Kind code of ref document: T

Owner name: INCYTE HOLDINGS CORPORATION, US

Effective date: 20240429